Variant DetailsVariant: nsv977956Internal ID | 18266475 | Landmark | | Location Information | | Cytoband | 16p11.2 | Allele length | Assembly | Allele length | hg38 | 39603 | hg19 | 39603 | hg18 | 39603 |
| Variant Type | CNV duplication | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2056517, nssv2056514, nssv2056369, nssv2056366, nssv2056364, nssv2056515, nssv2056516, nssv2056367, nssv2056365, nssv2056368 | Samples | HGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927 | Known Genes | LOC613037 | Method | Sequencing | Analysis | lineage specific fixed duplications | Platform | Not reported | Comments | | Reference | Sudmant_et_al_2013 | Pubmed ID | 23825009 | Accession Number(s) | nsv977956
| Frequency | Sample Size | 10 | Observed Gain | 10 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|
|