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Accession: PRJNA283135 ID: 283135

Homo sapiens (human)

Characterization of deletions of the HBB locus by array comparative genomic hybridization

See Genome Information for Homo sapiens
Array-CGH used to characterize HBB deletions causing beta thalassemia and HPFH Overall design: Two-color experiment comparing thalssemia/HPFH subjects with normal DNA
AccessionPRJNA283135; GEO: GSE68587
Data TypeVariation
ScopeMultiisolate
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
PublicationsSabath DE et al., "Characterization of Deletions of the HBA and HBB Loci by Array Comparative Genomic Hybridization.", J Mol Diagn, 2016 Jan;18(1):92-9
SubmissionRegistration date: 5-May-2015
325 9th Ave, Laboratory Medicine, University of Washington
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Publications
PubMed1
PMC1
Other datasets
GEO DataSets1
GEO Data Details
ParameterValue
Data volume, Spots173184
Data volume, Processed Mbytes4
Data volume, Supplementary Mbytes48

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