Variant DetailsVariant: nsv545245Internal ID | 15985968 | Landmark | | Location Information | | Cytoband | 1p36.31 | Allele length | Assembly | Allele length | hg38 | 6385 | hg19 | 6385 | hg18 | 6385 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv77n54 | Supporting Variants | nssv709162, nssv709164, nssv709161, nssv709163, nssv709165 | Samples | | Known Genes | ACOT7 | 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) | nsv545245
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 5 | Observed Complex | 0 | Frequency | n/a |
|
|