Variant DetailsVariant: nsv568662Internal ID | 16009385 | Landmark | | Location Information | | Cytoband | 15q12 | Allele length | Assembly | Allele length | hg38 | 1329631 | hg19 | 1376688 | hg18 | 1490385 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv839289 | Samples | | Known Genes | APBA2, GOLGA6L7P, GOLGA8F, GOLGA8G, GOLGA8M, HERC2, HERC2P9, LOC100289656, LOC646278, MIR4509-1, MIR4509-2, MIR4509-3, OCA2, WHAMMP2 | Method | SNP array | Analysis | Illumina SNP array copy number analysis | Platform | Not reported | Comments | | Reference | Cooper_et_al_2011 | Pubmed ID | 21841781 | Accession Number(s) | nsv568662
| Frequency | Sample Size | 17421 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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