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Status
Public on Oct 03, 2012
Title
[CytoScanHD_Array] Affymetrix CytoScan HD Array
Technology type
in situ oligonucleotide
Distribution
commercial
Organism
Homo sapiens
Manufacturer
Affymetrix
Manufacture protocol
see manufacturer's web site
Description
#%create_date=2011-12-01 GMT-08:00 10:25:44 #%chip_type=CytoScanHD_Array #%genome-species=Homo sapiens #%genome-version=hg19 #%genome-version-ucsc=hg19 #%genome-version-ncbi=GRCh37 #%genome-version-create_date=2009-02-00 #%dbSNP_date=2010-09-23 #%dbSNP_version=132 #%dgv-date=2010-10-00 #%dgv-version=10 #%hapmap-date=2008-01-08 #%hapmap-version=23 #%netaffx-annotation-date=2011-12-01 #%netaffx-annotation-netaffx-build=32.1 #%netaffx-annotation-tabular-format-version=1.0 #%netaffx-annotation-docgen-method=com.affymetrix.database.docgen.DocGenDriver #%netaffx-annotation-docgen-version=cluster_friendly_submission #%create_date=2011-12-01 GMT-08:00 10:25:09 #%chip_type=CytoScanHD_Array #%genome-species=Homo sapiens #%genome-version=hg19 #%genome-version-ucsc=hg19 #%genome-version-ncbi=GRCh37 #%genome-version-create_date=2009-02-00 #%dbSNP_date=2010-09-23 #%dbSNP_version=132 #%dgv-date=2010-10-00 #%dgv-version=10 #%netaffx-annotation-date=2011-12-01 #%netaffx-annotation-netaffx-build=32.1 #%netaffx-annotation-tabular-format-version=1.0 #%netaffx-annotation-docgen-method=com.affymetrix.database.docgen.DocGenDriver #%netaffx-annotation-docgen-version=cluster_friendly_submission ##This database/product contains information from the Online Mendelian Inheritance in Man(R) (OMIM(R)) database, which has been obtained under a license from the Johns Hopkins University. This database/product does not represent the entire, unmodified OMIM(R) database, which is availa ble in its entirety at www.ncbi.nlm.nih.gov/omim/.
Web link
http://www.affymetrix.com/support/technical/byproduct.affx?product=cytoscan_kit
Submission date
Oct 03, 2012
Last update date
Jul 13, 2018
Organization
Affymetrix, Inc.
E-mail(s)
geo@ncbi.nlm.nih.gov, support@affymetrix.com
Phone
888-362-2447
URL
http://www.affymetrix.com/index.affx
Street address
City
Santa Clara
State/province
CA
ZIP/Postal code
95051
Country
USA
Samples (6974)
GSM1014057 , GSM1019673 , GSM1019674 , GSM1019675 , GSM1019676 , GSM1019677
GSM1019678 ,
GSM1019679 ,
GSM1019680 ,
GSM1019681 ,
GSM1019682 ,
GSM1019683 ,
GSM1019684 ,
GSM1146803 ,
GSM1146804 ,
GSM1146805 ,
GSM1146806 ,
GSM1146807 ,
GSM1146808 ,
GSM1146809 ,
GSM1146810 ,
GSM1146811 ,
GSM1146812 ,
GSM1146813 ,
GSM1146814 ,
GSM1146815 ,
GSM1146816 ,
GSM1146817 ,
GSM1146818 ,
GSM1146819 ,
GSM1146820 ,
GSM1146821 ,
GSM1146822 ,
GSM1146823 ,
GSM1146824 ,
GSM1146825 ,
GSM1146826 ,
GSM1146827 ,
GSM1146828 ,
GSM1146829 ,
GSM1146830 ,
GSM1146831 ,
GSM1146832 ,
GSM1199922 ,
GSM1199923 ,
GSM1199924 ,
GSM1199925 ,
GSM1199926 ,
GSM1199927 ,
GSM1223764 ,
GSM1223765 ,
GSM1223766 ,
GSM1223767 ,
GSM1223768 ,
GSM1223769 ,
GSM1223770 ,
GSM1223771 ,
GSM1223772 ,
GSM1223773 ,
GSM1223774 ,
GSM1223775 ,
GSM1223776 ,
GSM1277820 ,
GSM1277821 ,
GSM1277822 ,
GSM1277823 ,
GSM1277824 ,
GSM1277825 ,
GSM1277826 ,
GSM1277827 ,
GSM1277828 ,
GSM1277829 ,
GSM1277830 ,
GSM1277831 ,
GSM1277832 ,
GSM1277833 ,
GSM1277834 ,
GSM1300967 ,
GSM1300968 ,
GSM1300969 ,
GSM1300970 ,
GSM1300971 ,
GSM1300972 ,
GSM1300973 ,
GSM1300974 ,
GSM1300975 ,
GSM1300976 ,
GSM1300977 ,
GSM1300978 ,
GSM1300979 ,
GSM1300980 ,
GSM1300981 ,
GSM1300982 ,
GSM1300983 ,
GSM1300984 ,
GSM1300985 ,
GSM1300986 ,
GSM1300987 ,
GSM1300988 ,
GSM1300989 ,
GSM1300990 ,
GSM1300991 ,
GSM1300992 ,
GSM1300993 ,
GSM1300994 ,
GSM1300995 ,
GSM1300996 ,
GSM1300997 ,
GSM1300998 ,
GSM1300999 ,
GSM1301000 ,
GSM1301001 ,
GSM1301002 ,
GSM1301003 ,
GSM1301004 ,
GSM1301005 ,
GSM1301006 ,
GSM1301007 ,
GSM1301008 ,
GSM1301009 ,
GSM1301010 ,
GSM1301011 ,
GSM1317174 ,
GSM1317175 ,
GSM1317176 ,
GSM1317177 ,
GSM1317178 ,
GSM1317179 ,
GSM1317180 ,
GSM1317181 ,
GSM1317182 ,
GSM1317183 ,
GSM1317184 ,
GSM1317185 ,
GSM1317186 ,
GSM1317187 ,
GSM1317188 ,
GSM1317189 ,
GSM1317190 ,
GSM1317191 ,
GSM1317192 ,
GSM1317193 ,
GSM1317194 ,
GSM1317195 ,
GSM1317196 ,
GSM1317197 ,
GSM1317198 ,
GSM1317199 ,
GSM1317200 ,
GSM1317201 ,
GSM1317202 ,
GSM1317203 ,
GSM1317204 ,
GSM1317205 ,
GSM1317206 ,
GSM1317207 ,
GSM1317208 ,
GSM1317209 ,
GSM1317210 ,
GSM1317211 ,
GSM1317212 ,
GSM1317213 ,
GSM1317214 ,
GSM1317215 ,
GSM1317216 ,
GSM1317217 ,
GSM1317218 ,
GSM1317219 ,
GSM1317220 ,
GSM1317221 ,
GSM1317222 ,
GSM1317223 ,
GSM1317224 ,
GSM1317225 ,
GSM1317226 ,
GSM1317227 ,
GSM1317228 ,
GSM1317229 ,
GSM1317230 ,
GSM1317231 ,
GSM1317232 ,
GSM1317233 ,
GSM1317234 ,
GSM1317235 ,
GSM1317236 ,
GSM1317237 ,
GSM1317238 ,
GSM1317239 ,
GSM1317240 ,
GSM1317241 ,
GSM1317242 ,
GSM1317243 ,
GSM1317244 ,
GSM1317245 ,
GSM1317246 ,
GSM1317247 ,
GSM1317248 ,
GSM1317249 ,
GSM1317250 ,
GSM1317251 ,
GSM1317252 ,
GSM1317253 ,
GSM1317254 ,
GSM1317255 ,
GSM1317256 ,
GSM1317257 ,
GSM1317258 ,
GSM1317259 ,
GSM1317260 ,
GSM1317261 ,
GSM1317262 ,
GSM1317263 ,
GSM1317264 ,
GSM1317265 ,
GSM1317266 ,
GSM1317267 ,
GSM1317268 ,
GSM1317269 ,
GSM1317270 ,
GSM1317271 ,
GSM1317272 ,
GSM1317273 ,
GSM1317274 ,
GSM1317275 ,
GSM1317276 ,
GSM1317277 ,
GSM1317278 ,
GSM1317279 ,
GSM1317280 ,
GSM1317281 ,
GSM1317282 ,
GSM1317283 ,
GSM1317284 ,
GSM1317285 ,
GSM1317286 ,
GSM1317287 ,
GSM1317288 ,
GSM1317289 ,
GSM1317290 ,
GSM1317291 ,
GSM1317292 ,
GSM1317293 ,
GSM1317294 ,
GSM1317295 ,
GSM1317296 ,
GSM1317297 ,
GSM1317298 ,
GSM1317299 ,
GSM1317300 ,
GSM1317301 ,
GSM1317302 ,
GSM1317303 ,
GSM1317304 ,
GSM1317305 ,
GSM1317306 ,
GSM1317307 ,
GSM1317308 ,
GSM1317309 ,
GSM1317310 ,
GSM1317311 ,
GSM1317312 ,
GSM1317313 ,
GSM1317314 ,
GSM1317315 ,
GSM1317316 ,
GSM1317317 ,
GSM1317318 ,
GSM1317319 ,
GSM1317320 ,
GSM1317321 ,
GSM1317322 ,
GSM1317323 ,
GSM1317324 ,
GSM1317325 ,
GSM1317326 ,
GSM1317327 ,
GSM1317328 ,
GSM1317329 ,
GSM1317330 ,
GSM1317331 ,
GSM1317332 ,
GSM1317333 ,
GSM1317334 ,
GSM1317335 ,
GSM1317336 ,
GSM1317337 ,
GSM1317338 ,
GSM1317339 ,
GSM1317340 ,
GSM1317341 ,
GSM1317342 ,
GSM1317343 ,
GSM1317344 ,
GSM1317345 ,
GSM1317346 ,
GSM1317347 ,
GSM1317348 ,
GSM1317349 ,
GSM1317350 ,
GSM1317351 ,
GSM1317352 ,
GSM1317353 ,
GSM1317354 ,
GSM1317355 ,
GSM1317356 ,
GSM1317357 ,
GSM1317358 ,
GSM1317359 ,
GSM1317360 ,
GSM1317361 ,
GSM1317362 ,
GSM1317363 ,
GSM1317364 ,
GSM1317365 ,
GSM1317366 ,
GSM1317367 ,
GSM1317368 ,
GSM1317369 ,
GSM1317370 ,
GSM1317371 ,
GSM1317372 ,
GSM1317373 ,
GSM1317374 ,
GSM1317375 ,
GSM1317376 ,
GSM1317377 ,
GSM1317378 ,
GSM1317379 ,
GSM1317380 ,
GSM1317381 ,
GSM1317382 ,
GSM1317383 ,
GSM1317384 ,
GSM1317385 ,
GSM1317386 ,
GSM1317387 ,
GSM1317388 ,
GSM1317389 ,
GSM1317390 ,
GSM1317391 ,
GSM1317392 ,
GSM1317393 ,
GSM1317394 ,
GSM1317395 ,
GSM1317396 ,
GSM1317397 ,
GSM1317398 ,
GSM1317399 ,
GSM1317400 ,
GSM1317401 ,
GSM1317402 ,
GSM1317403 ,
GSM1317404 ,
GSM1317405 ,
GSM1317406 ,
GSM1317407 ,
GSM1317408 ,
GSM1317409 ,
GSM1317410 ,
GSM1317411 ,
GSM1317412 ,
GSM1317413 ,
GSM1317414 ,
GSM1317415 ,
GSM1317416 ,
GSM1317417 ,
GSM1317418 ,
GSM1317419 ,
GSM1317420 ,
GSM1317421 ,
GSM1317422 ,
GSM1317423 ,
GSM1317424 ,
GSM1317425 ,
GSM1317426 ,
GSM1317427 ,
GSM1317428 ,
GSM1317429 ,
GSM1317430 ,
GSM1317431 ,
GSM1317432 ,
GSM1317433 ,
GSM1317434 ,
GSM1317435 ,
GSM1317436 ,
GSM1317437 ,
GSM1317438 ,
GSM1317439 ,
GSM1317440 ,
GSM1317441 ,
GSM1317442 ,
GSM1317443 ,
GSM1317444 ,
GSM1317445 ,
GSM1317446 ,
GSM1317447 ,
GSM1317448 ,
GSM1317449 ,
GSM1317450 ,
GSM1317451 ,
GSM1317452 ,
GSM1317453 ,
GSM1317454 ,
GSM1317455 ,
GSM1317456 ,
GSM1317457 ,
GSM1317458 ,
GSM1317459 ,
GSM1317460 ,
GSM1317461 ,
GSM1317462 ,
GSM1317463 ,
GSM1317464 ,
GSM1317465 ,
GSM1317466 ,
GSM1317467 ,
GSM1317468 ,
GSM1317469 ,
GSM1317470 ,
GSM1317471 ,
GSM1317472 ,
GSM1317473 ,
GSM1317474 ,
GSM1317475 ,
GSM1317476 ,
GSM1317477 ,
GSM1317478 ,
GSM1317479 ,
GSM1317480 ,
GSM1317481 ,
GSM1317482 ,
GSM1317483 ,
GSM1317484 ,
GSM1317485 ,
GSM1317486 ,
GSM1317487 ,
GSM1317488 ,
GSM1317489 ,
GSM1317490 ,
GSM1317491 ,
GSM1317492 ,
GSM1317493 ,
GSM1317494 ,
GSM1317495 ,
GSM1317496 ,
GSM1317497 ,
GSM1317498 ,
GSM1317499 ,
GSM1317500 ,
GSM1317501 ,
GSM1317502 ,
GSM1317503 ,
GSM1317504 ,
GSM1317505 ,
GSM1317506 ,
GSM1317507 ,
GSM1317508 ,
GSM1317509 ,
GSM1317510 ,
GSM1317511 ,
GSM1317512 ,
GSM1317513 ,
GSM1317514 ,
GSM1317515 ,
GSM1317516 ,
GSM1317517 ,
GSM1317518 ,
GSM1317519 ,
GSM1317520 ,
GSM1317521 ,
GSM1317522 ,
GSM1317523 ,
GSM1317524 ,
GSM1317525 ,
GSM1317526 ,
GSM1317527 ,
GSM1317528 ,
GSM1317529 ,
GSM1317530 ,
GSM1317531 ,
GSM1317532 ,
GSM1317533 ,
GSM1317534 ,
GSM1317535 ,
GSM1317536 ,
GSM1317537 ,
GSM1317538 ,
GSM1317539 ,
GSM1317540 ,
GSM1317541 ,
GSM1317542 ,
GSM1317543 ,
GSM1317544 ,
GSM1317545 ,
GSM1317546 ,
GSM1317547 ,
GSM1317548 ,
GSM1317549 ,
GSM1317550 ,
GSM1317551 ...
Accession list truncated, click here to browse through all related public accessions You can also download a list of all accessions here
Series (169)
GSE41297
SNP array data for embryonal rhabdomyosarcoma in a patient with Costello syndrome
GSE41581
Frequent truncating mutations of STAG2 in bladder cancer
GSE47204
CytoScanHD array Data for Colerectal Tumor and Normal Samples
GSE49483
Phenotypic, genomic and functional characterization reveals no differences between CD138++ and CD138low subpopulations in multiple myeloma cell lines (Copy Number)
GSE50573
Posterior Amorphous Corneal Dystrophy Is Associated with a Deletion of Small Leucine-rich Proteoglycans on Chromosome 12
GSE52902
Impact of Gene Dosage on Gene Expression, Biological Processes and Survival in Cervical Cancer: a Genome-Wide Follow-Up Study [CytoScanHD_Array]
GSE52904
Impact of Gene Dosage on Gene Expression, Biological Processes and Survival in Cervical Cancer: a Genome-Wide Follow-Up Study
GSE53799
CytoScanHD array Data for 15 normal, 15 primary colorectal carcinomas and their 15 matched liver metastases
GSE54504
A Genomic Portrait of Resectable Hepatocellular Carcinomas: Implications of RB1 and FGF19 Aberrations for Patient Stratification.
GSE57943
aCGH/SNP data from Hepatosplenic T cell lymphoma patient samples
GSE57944
Hepatosplenic T cell lymphoma
GSE58694
Affymetrix CytoScan HD array data for patient with Intellectual Disabilities
GSE58781
Retinoblastoma SNP array data
GSE58785
Pan-genomic study of primary human retinoblastoma samples
GSE58793
De novo homozygous deletion of segmental KAL1 and entire STS cause Kallmann syndrome and X-linked ichthyosis in a Chinese family
GSE59150
A High-Resolution Copy Number Variation Resource for Clinical Genetics
GSE59298
METRONOMIC TOPOTECAN CAUSES THERAPY-INDUCED TUMOR CELL SENESCENCE AND LOSS OF AGGRESSIVE PROPERTIES IN MYCN-AMPLIFIED CHILDHOOD CANCER
GSE59529
METRONOMIC TOPOTECAN CAUSES THERAPY-INDUCED TUMOR CELL SENESCENCE AND LOSS OF AGGRESSIVE PROPERTIES IN MYCN-AMPLIFIED CHILDHOOD CANCER [Affymetrix Cytoscan HD]
GSE59537
Bone marrows from neuroblastoma patients: an excellent source for tumor genome analyses
GSE60218
Affymetrix SNP array data of melanoma cell lines
GSE60720
Affymetrix SNP array data for cone precursor derived retinoblastoma like samples
GSE60733
Affymetrix SNP array data for NUP98 rearranged acute leukemias
GSE61594
Copy number variation analysis of pheochromocytoma and paraganglioma
GSE63028
7q11.23 dosage-dependent dysregulation in the human pluripotent state primes aberrant transcriptional programs in disease-relevant lineages (aCGH)
GSE63058
7q11.23 dosage-dependent dysregulation in the human pluripotent state primes aberrant transcriptional programs in disease-relevant lineages
GSE63891
Affymetrix SNP array data for rhabdomyosarcoma samples
GSE65113
CNV and ROH analysis of patients with a region of triplication followed by a terminal region of ROH and their parental samples
GSE66422
SNP array of human neuroblastoma cell lines SH-SY5Y, SH-EP and SK-N-SH
GSE67125
Affymetrix CytoscanHD data for genomic plasticity of osteosarcoma cell lines
GSE67460
Affymetrix SNP array data for chronic myelomonocytic leukemia samples
GSE68078
Cytoscan HD arrays data for Nodal marginal zone lymphoma (NMZL)
GSE69161
Integrative analysis of copy number and gene expression data suggests novel pathogenic mechanisms in Primary Myelofibrosis
GSE69613
Affymetrix Cytoscan HD Array Data for a patient with Partial Androgen Insensitivity Syndrome and Recto Sigmoid Cancer: a family study
GSE69632
Effects of Integrating and Non-integrating Reprogramming Methods on Copy Number Variation and Genomic Stability of Human Induced Pluripotent Stem Cells
GSE72209
CNA data from The human glioblastoma cell culture resource: validated cell models representing all molecular subtypes
GSE72219
The human glioblastoma cell culture resource
GSE72667
Rare CNVs in Lynch Syndrome patients negative for mutations in mismatch repair genes [Affymetrix]
GSE72668
Rare CNVs in Lynch Syndrome patients negative for mutations in mismatch repair genes
GSE73976
Affymetrix SNP array data of 35 multiple myeloma patients from UZ Leuven (Belgium)
GSE74239
Affymetrix CytoScan HD array data for del(17p) Chronic Lymphocytic Leukemia samples
GSE76100
Patient-derived xenografts from pediatric liver cancer predict tumor recurrence and advise clinical management
GSE76436
Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variation.
GSE76438
Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variation.
GSE77138
Large genomic alteration of 7q in two patients with multiple primary cancers, including triple negative breast cancer, and family history of malignant neoplasms
GSE77275
CNV analysis of hepatocellular carcinoma with portal vein tumor thrombosis
GSE77276
The molecular landscape of hepatocellular carcinoma with portal vein tumor thrombosis
GSE77368
SNP arrays of tumors derived from human prostate epithelial cells transformed with the oncogenes N-Myc and myrAKT1
GSE77995
Affymetrix CytoScan HD array data of iPSCs and iPSC-derived-NSPCs
GSE78808
Chromosomal abnormalities in hepatic cysts point to novel polycystic liver disease genes
GSE79187
Tumor Touch Imprints as Source for Whole Genome Analysis of Neuroblastoma Tumors
GSE80208
CNV anlysis of human parthenogenetic haploid ESCs (hPGES)
GSE80736
Affymetrix SNP array data of melanoma cell lines from lymph node metastates
GSE80813
De novo and rare inherited copy-number variations in the hemiplegic form of cerebral palsy
GSE81025
Genomic analysis of human parthenogenetic haploid ESCs (hPGES), normal human ESCs(H9) and human forskin fibroblast
GSE83089
Copy number variation data from iPS cells with PTCHD1-AS deletions
GSE84291
Impact of disseminated neuroblastoma cells on the identification of the relapse seeding clone
GSE84810
Improving the Positive Predictive Value of Non-invasive Prenatal Screening (NIPS)
GSE85586
Genomic alterations in MPT patients with multiple primary tumors
GSE85937
Genome profiling of free circulating tumor DNA by oncoscan and comparison to profiles in tumor biopsies evaluated by cytoscan
GSE87802
Individuals with excess numbers of germline de novo CNVs [Affymetrix]
GSE87915
Individuals with excess numbers of germline de novo CNVs
GSE89398
Clonal variation in drug and radiation response among glioma-initiating cells is linked to proneural-mesenchymal transition (CytoScanHD)
GSE89401
Clonal variation in drug and radiation response among glioma-initiating cells is linked to proneural-mesenchymal transition
GSE89616
Copy number analysis of plasma cells from AL amyloidosis patients
GSE93077
Affymetrix Cytoscan HD 2,600K SNP array data for 9 GISTs
GSE93286
Proteogenomic characterization and comprehensive integrative genomic analysis of human colorectal cancer liver metastasis
GSE93328
Decreased CTCF Expression Directs DNA Hypermethylation Events in Cancer
GSE93364
DNA methylation and gene expression after decreased CTCF expression in human prostate epithelial cells
GSE93886
Marker chromosomes can arise from chromothripsis and predict adverse prognosis in acute myeloid leukemia
GSE94378
Intra and inter-tumoral heterogeneity in syndromic neuroendocrine tumors
GSE94705
Integrating genomic alterations in diffuse large B-cell Lymphoma identifies new relevant pathways and potential therapeutic targets
GSE95085
Affymetrix CytoScan® HD Array (SNP and copy number array) used on pseudarthrosis tissue from Neurofibromatosis type 1 individuals
GSE96884
Affymetrix SNP array data of melanoma cell lines II
GSE96897
Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans [AffymetrixCytoScanHD]
GSE96909
Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans
GSE97436
Affymetrix SNP array data for chronic lymphoblastic leukemia samples
GSE100844
SAMHD1 is recurrently mutated in T-cell prolymphocytic leukemia
GSE101110
Detailed Longitudinal Sampling of Glioma Stem Cells In Situ Reveals Chr7 Gain and Chr10 Loss As Repeated Events in Primary Tumor Formation and Recurrence (SNP)
GSE101114
Detailed Longitudinal Sampling of Glioma Stem Cells In Situ Reveals Chr7 Gain and Chr10 Loss As Repeated Events in Primary Tumor Formation and Recurrence
GSE101414
Genome-wide copy number variation analysis identifies novel candidate loci associated with pediatric obesity [CytoScanHD_Array]
GSE101418
Genome-wide copy number variation analysis identifies novel candidate loci associated with pediatric obesity
GSE101533
Deletion of 11q in neuroblastomas drives sensitivity to PARP inhibition [SNP array]
GSE101990
Deletion of 11q in neuroblastomas drives sensitivity to PARP inhibition
GSE106818
Impact of IQ on the diagnostic yield of chromosomal microarray in a community sample of adults with schizophrenia
GSE108009
CYTOGENETIC AND TRANSCRIPTOME PROFILING ANALYSIS OF MATCHED IN SITU/INVASIVE CUTANEOUS SQUAMOUS CELL CARCINOMAS FROM IMMUNOCOMPETENT PATIENTS [CytoScanHD_Array]
GSE108010
CYTOGENETIC AND TRANSCRIPTOME PROFILING ANALYSIS OF MATCHED IN SITU/INVASIVE CUTANEOUS SQUAMOUS CELL CARCINOMAS FROM IMMUNOCOMPETENT PATIENTS
GSE108085
Comprehensive molecular profiling of children with recurrent cancer I
GSE108089
Comprehensive molecular profiling of children with recurrent cancer
GSE109046
Comparison of expression data from DLD-1 subpopulations III
GSE109047
Comparison of expression data from DLD-1 subpopulations
GSE112111
CytoScan HD array data for a patient with Vitamin D deficiency
GSE113384
Effect of EGC treatment on genome instability induced by cisplatin treatment
GSE114870
Affymetrix CytoScan HD for autism spectrum disorder in children
GSE115666
Interrupted reprogramming into induced pluripotent stem cells does not rejuvenate human mesenchymal stromal cells
GSE116522
Burkitt-like lymphoma with 11q aberration: A germinal center derived lymphoma without ID3-TCF3-CCND3 pathway deregulation [CYTOSCAN]
GSE116527
Burkitt-like lymphoma with 11q aberration: A germinal center derived lymphoma without ID3-TCF3-CCND3 pathway deregulation
GSE117093
Gastric cancer samples of Mexican patients
GSE118477
Affymetrix SNP array data for dic(1;7)(q10;p10) in Myelodysplastic Syndromes (MDS)
GSE118648
A Distinct Epigenetic Program Underlies the 1;7 Translocation in Myelodysplastic Syndromes (MDS)
GSE120007
Affymetrix SNP array data of a TRNT1 positive MDS adult patient
GSE120624
Affymetrix CytoScan 750K and HD data for developmental delay and/or physical disability phenotypes samples
GSE122584
Phenotypic cooperation of a KCNQ2 exon 7 partial duplication and compound copy number variations in genes associated to a severe epileptic and neurodevelopmental delay
GSE122859
Affymetrix SNP array data for a pediatric acute lymphoblastic leukemia samples
GSE123682
CNV analysis of normal brain and glioma samples
GSE124330
Copy number (SNP) analysis from leukemic patients with complex structural variants
GSE128214
Large B-Cell Lymphomas in Pediatric and Young Adults Display Clinically Relevant Molecular Features Distinguishable from Adult Counterparts [cytoscan]
GSE128294
Large B-Cell Lymphomas in Pediatric and Young Adults Display Clinically Relevant Molecular Features Distinguishable from Adult Counterparts
GSE132088
Genomic alteration analysis in ovarian cancers
GSE132218
Epigenetic footprint of hepatoblastoma defines a novel integrative molecular classification with clinical implications [CytoScanHD_Array]
GSE132219
Epigenetic footprint of hepatoblastoma defines a novel integrative molecular classification with clinical implications
GSE132453
Comorbidities - microcephaly, facial dysmorphia and epilepsy - increase the risk of the pathogenic CNV finding in patients with intellectual disability and autism
GSE133063
A Novel Silent Mutation in the L1CAM Gene causing Fetal Hydrocephalus
GSE133150
Affymetrix SNP array data for a Diffuse Large B-cell Lymphoma case with a TERT promoter variant who later developed Chronic Myelomonocytic Leukemia
GSE134349
Copy number variations analysis by CytoscanHD array of 33 human pleural mesothelioma cell lines
GSE136297
CytoScan HD array data from Human mammary epithelian cells after Cyclin E overexpression
GSE138489
Heterozygous deletion of the SHOX gene enhancer in two females with clinical heterogeneity associating with skewed XCI and escaping XCI
GSE143232
Affymetrix CytoScan array data for leukemia cell lines
GSE144015
Microarray data for inflammatory breast cancer cases
GSE144446
Affymetrix CytoScan array data for leukemia cell lines TK6 and WIL2-NS
GSE145901
Comprehensive genomic profiling of undifferentiated embryonic sarcoma of the liver
GSE146554
Global DNA hypomethylation in ovarian cancer (CNV_data)
GSE146556
Global DNA hypomethylation in ovarian cancer
GSE147280
ChIP-chip by SNP array of a case of a patient with TCF3-HLF-positive BCP-ALL
GSE147381
Clinical significance of recurrent copy number abnormalities revealed by SNP array in childhood T-cell acute lymphoblastic leukemia
GSE147773
Malignant Schwann cell precursors mediate intratumoral plasticity in human neuroblastoma [Array]
GSE147777
Malignant Schwann cell precursors mediate intratumoral plasticity in human neuroblastoma
GSE148229
Chromosomal instability associated with adverse outcome: a case report of patient with Nijmegen breakage syndrome and rapidly developed T-NHL with complex karyotype
GSE149038
Copy number data from Patient-Derived tumor models (PDX) establish from bone metastases of breast cancer.
GSE151766
Multiple chromoanasynthesis in a rare case of sporadic renal leiomyosarcoma: case report
GSE152178
Affymetric SNP Array Data of 45 liver metastasis samples from colorectal cancer patients
GSE154591
Genomic comparison of post-radiation versus sporadic sarcomas
GSE154830
Overlap Between Pediatric Nodal Marginal Zone Lymphoma (PNMZL) and Pediatric-Type Follicular Lymphoma (PTFL) : Morphological and Molecular Analysis (CytoScan)
GSE154834
Overlap Between Pediatric Nodal Marginal Zone Lymphoma (PNMZL) and Pediatric-Type Follicular Lymphoma (PTFL) : Morphological and Molecular Analysis
GSE157845
Spontaneous Cell Fusions as a Mechanism of Parasexual Recombination in Tumor Cell Populations.
GSE160569
Characterization of Mutational Status, Spheroid Formation, and Drug Response of a New Genomically-Stable Human Ovarian Clear Cell Carcinoma Cell Line, 105C (Affymetrix)
GSE160571
Characterization of Mutational Status, Spheroid Formation, and Drug Response of a New Genomically-Stable Human Ovarian Clear Cell Carcinoma Cell Line, 105C
GSE160982
SNP array of 121 AML patients at diagnosis
GSE161275
CNV analysis of normal brain and glioma samples II
GSE162000
Affymetrix SNP array data for acute leukemias with a 14q32/BCL11B rearrangement
GSE162283
14q32 recombinations deregulating BCL11B mark a distinct Mixed Phenotype Leukemia
GSE163134
SNParray data for banking lines in Korea National Stem Cell Bank
GSE164554
CytoScan HD array for multiple myeloma samples
GSE178261
Hypodiploidy in a pediatric patient of T-cell acute lymphoblastic leukemia: a case report
GSE178421
Global genetic profiling of a pediatric series of T-cell lymphoblastic lymphoma [Cytoscan]
GSE178427
Global genetic profiling of a pediatric series of T-cell lymphoblastic lymphoma
GSE178731
THP-1 cell lines: reference data for classification of THP-1 cells [genome]
GSE178741
THP-1 cell lines: reference data for classification of THP-1 cells
GSE182785
Affymetrix SNP array data for Myeloid Neoplasms with PDGFRB Rearrangement
GSE182820
Genomic and Clinical Findings in Myeloid Neoplasms with PDGFRB Rearrangement
GSE185165
Affymetrix CytoScan HD and OncoScan array data for malignant melanoma samples
GSE192614
Affymetrix SNP array data for preeclampsia samples
GSE193017
SNP array data for Wilms Tumor harboring de novo germline mutation in CTCF
GSE193235
Germline Variant in *Ctcf* Links Mental Retardation to Wilms Tumor Predisposition
GSE197838
Affymetrix SNP array data for acute lymphoblastic leukemia samples
GSE205269
Chromothripsis is a frequent event and underlies typical genetic changes in early T-cell precursor lymphoblastic leukemia in adults [SNP]
GSE205270
Chromothripsis is a frequent event and underlies typical genetic changes in early T-cell precursor lymphoblastic leukemia in adults
GSE209728
Affymetrix CytoScan HD data on neuroblastoma cell lines
GSE216574
Double-deletion of 1p32 defines ultra-high-risk myeloma, but monoallelic del(1p32) remains a strong prognostic factor
GSE231621
Copy Number Variation data from non-trasformed human fibroblasts
GSE240546
Comparison of CNV in 6 ostosarcoma cell lines
GSE243055
A novel t(X;21) (p11.4;q22.12) translocation adds to the role of BCOR and RUNX1 in Myelodysplastic Syndromes/Acute Myeloid Leukemias [Copy number analysis]
GSE243056
A novel t(X;21) (p11.4;q22.12) translocation adds to the role of BCOR and RUNX1 in Myelodysplastic Syndromes/Acute Myeloid Leukemias
GSE243782
K-562 cell lines
GSE252947
MYC-rearranged aggressive B-cell lymphoma are molecularly Burkitt Lymphoma despite of morphology [CYTOSCAN]
GSE252974
MYC-rearranged aggressive B-cell lymphoma are molecularly Burkitt Lymphoma despite of morphology.
GSE267970
Affymetrix SNP array data for T-cell acute lymphoblastic leukemia samples
GSE269220
Comprehensive Analysis of Relapsed-Refractory Mature B-cell Non-Hodgkin Lymphoma in Children and Adolescents
GSE270110
Copy number variants in autism spectrum disorders
GSE282080
imprinting disorders: Beckwith–Wiedemann, Silver–Russell, and Prader-Willi syndromes in Egyptian patients
Data table header descriptions
ID
dbSNP RS ID
Chromosome
Physical Position
Strand
SPOT_ID
RANGE_GB
RANGE_START
RANGE_END
Data table
ID
dbSNP RS ID
Chromosome
Physical Position
Strand
SPOT_ID
RANGE_GB
RANGE_START
RANGE_END
S-3AAFK
rs1466535
12
57534470
-
rs1466535
S-3AAFJ
rs72925282
4
83904997
+
rs72925282
S-3AAFI
rs2826163
21
21683874
+
rs2826163
S-3AAFH
rs176264
14
29162832
+
rs176264
S-3AAFG
rs524692
6
125419899
-
rs524692
S-3AAFF
3
97713361
+
chr 3: 40901503
S-3AAFE
rs62414793
6
62948241
+
rs62414793
S-3AAFD
rs72704195
4
175490632
+
rs72704195
S-3AAFC
2
40901503
+
chr 2: 68072527
S-3AAFB
rs10519437
5
115323724
+
rs10519437
S-3AAFA
rs379462
3
52004317
-
rs379462
S-3AAEZ
rs3784711
15
68072527
+
rs3784711
S-3AAEY
rs17236705
8
63095157
+
rs17236705
S-3AAEX
rs17564689
22
46006110
+
rs17564689
S-3AAEW
rs1112258
15
26574330
+
rs1112258
S-3AAEV
rs58172940
9
106367911
+
rs58172940
S-3AAEU
rs41334344
12
41011120
-
rs41334344
S-3AAET
7
31936704
+
chr 7: 73568191
S-3AAES
rs62299785
4
5509714
+
rs62299785
S-3AAER
rs709551
3
107079175
+
rs709551
Total number of rows: 2822125 Table truncated, full table size 173648 Kbytes .
Supplementary data files not provided