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Copy number variation data from iPS cells with PTCHD1-AS deletions

ABSTRACT: iPS cell lines were generated from a male with ASD (proband or prb) and his unaffected mother (control or ctrl). Both individuals carry X-linked 167kb microdeletions that disrupt both PTCHD1 and PTCHD1-AS. We found that cells PTCHD1/PTCHD1-AS-null cells tended to have abnormal karyotypes. Copy number variation analyses were performed to examine genomic stability in control and proband iPS cell lines.

ORGANISM(S): Homo sapiens

PROVIDER: GSE83089 | GEO | 2019/05/18

REPOSITORIES: GEO

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