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Accession: PRJNA166921 ID: 166921

Homo sapiens (human)

X-linked CNV burden and male infertility

See Genome Information for Homo sapiens
Male factor infertility affects about 7% of men in the general population and it can be related to a number of different etiologic factors, including genetic anomalies. More...
AccessionPRJNA166921; GEO: GSE37948
Data TypeVariation
ScopeMultiisolate
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
PublicationsKrausz C et al., "High resolution X chromosome-specific array-CGH detects new CNVs in infertile males.", PLoS One, 2012;7(10):e44887
SubmissionRegistration date: 11-May-2012
Univerity of Florence
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Publications
PubMed1
PMC1
Other datasets
GEO DataSets1
GEO Data Details
ParameterValue
Data volume, Spots12584978
Data volume, Processed Mbytes280
Data volume, Supplementary Mbytes1283

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    X-linked CNV burden and male infertility
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