Variant DetailsVariant: nsv517068Internal ID | 15097675 | Landmark | | Location Information | | Cytoband | 15q24.3 | Allele length | Assembly | Allele length | hg38 | 126678 | hg19 | 126679 | hg18 | 126679 | hg17 | 126679 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv697047, nssv682226, nssv682321, nssv661383, nssv693432, nssv661834, nssv665263, nssv692990, nssv683277, nssv697169, nssv685115, nssv692684, nssv674633, nssv653725 | Samples | | Known Genes | PSTPIP1, TSPAN3 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv517068
| Frequency | Sample Size | 2026 | Observed Gain | 1 | Observed Loss | 13 | Observed Complex | 0 | Frequency | n/a |
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