Variant DetailsVariant: nsv568864Internal ID | 16009587 | Landmark | | Location Information | | Cytoband | 15q13.3 | Allele length | Assembly | Allele length | hg38 | 289698 | hg19 | 289698 | hg18 | 289698 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv839713 | Samples | | Known Genes | CHRNA7, GOLGA8K, ULK4P1, ULK4P2, ULK4P3 | 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) | nsv568864
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
|
|