Variant DetailsVariant: nsv614572 Internal ID | 16055295 | Landmark | | Location Information | | Cytoband | 9q21.11 | Allele length | Assembly | Allele length | hg38 | 18912 | hg19 | 18912 | hg18 | 18912 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv1137108, nssv1176077, nssv1137113, nssv1176079, nssv1176083, nssv1137109, nssv1176072, nssv1176071, nssv1137115, nssv1176070, nssv1176074, nssv1137107, nssv1137111, nssv1176069, nssv1137105, nssv1176082, nssv1176073, nssv1137106, nssv1137110, nssv1176080, nssv1176076, nssv1137116, nssv1176075, nssv1176081, nssv1137112, nssv1137114, nssv1176078 | Samples | HGDP00571, HGDP00167, HGDP00579, 1780862345_A, HGDP00454, HGDP01088, HGDP00460, 1780862043_A, HGDP00727, HGDP00203, HGDP01343, HGDP00688, HGDP00557, HGDP01294, HGDP00125 | Known Genes | APBA1 | 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) | nsv614572
| Frequency | Sample Size | 17421 | Observed Gain | 4 | Observed Loss | 23 | Observed Complex | 0 | Frequency | n/a |
|
|