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Accession: PRJNA339134 ID: 339134

Homo sapiens (human)

Identification of rare copy number polymorphic gains at 3q12.2 and 19q13.2 identifies candidate genes for familial endometriosis

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The association between endometriosis, genomic copy number variant polymorphisms and differential gene expression is still unclear. More...
AccessionPRJNA339134; GEO: GSE85701
Data TypeVariation
ScopeMultiisolate
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
SubmissionRegistration date: 16-Aug-2016
Human Molecular Cytogenetics, Genetics, USP
RelevanceMedical
Project Data:
Resource NameNumber
of Links
GEO DataSets1
GEO Data Details
ParameterValue
Data volume, Spots4623168
Data volume, Processed Mbytes72
Data volume, Supplementary Mbytes1306

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