Variant DetailsVariant: nsv579913Internal ID | 16020636 | Landmark | | Location Information | | Cytoband | 19q13.33 | Allele length | Assembly | Allele length | hg38 | 39674 | hg19 | 39674 | hg18 | 39674 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv1150655 | Samples | 1780862432_A | Known Genes | FLJ26850, VRK3, ZNF473 | 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) | nsv579913
| Frequency | Sample Size | 17421 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|
|