Variant DetailsVariant: nsv579337Internal ID | 16020060 | Landmark | | Location Information | | Cytoband | 19q13.11 | Allele length | Assembly | Allele length | hg38 | 652 | hg19 | 652 | hg18 | 652 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv6406n54 | Supporting Variants | nssv898549, nssv898551, nssv898546, nssv898554, nssv898552, nssv898548, nssv898553, nssv898550, nssv898547 | Samples | | Known Genes | CHST8 | 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) | nsv579337
| Frequency | Sample Size | 17421 | Observed Gain | 9 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|
|