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Accession: PRJNA170042 ID: 170042

Homo sapiens (human)

Detection of non-coding deletion CNVs upstream to FOXF1 [Agilent-022084]

See Genome Information for Homo sapiens
Genomic copy number analysis in patients with ACD/MPV. An unanticipated and tremendous amount of the non-coding sequences of the human genome are transcribed. More...
AccessionPRJNA170042; GEO: GSE38978
Data TypeVariation
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
PublicationsSzafranski P et al., "Small noncoding differentially methylated copy-number variants, including lncRNA genes, cause a lethal lung developmental disorder.", Genome Res, 2013 Jan;23(1):23-33
SubmissionRegistration date: 6-Jul-2012
Clinical genetics, ErasmusMC
Project Data:
Resource NameNumber
of Links
Other datasets
GEO DataSets1
GEO Data Details
Data volume, Spots86420
Data volume, Processed Mbytes2
Data volume, Supplementary Mbytes9

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  • Homo sapiens
    Homo sapiens
    Detection of non-coding deletion CNVs upstream to FOXF1 [Agilent-022084]

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