Variant DetailsVariant: nsv977903Internal ID | 18266422 | Landmark | | Location Information | | Cytoband | 16p13.13 | Allele length | Assembly | Allele length | hg38 | 5376 | hg19 | 5376 | hg18 | 5376 |
| Variant Type | CNV duplication | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2043638, nssv2043633, nssv2043636, nssv2043634, nssv2043629, nssv2043632, nssv2043637, nssv2043635, nssv2043630, nssv2043631 | Samples | HGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927 | Known Genes | CLEC16A | Method | Sequencing | Analysis | lineage specific fixed duplications | Platform | Not reported | Comments | | Reference | Sudmant_et_al_2013 | Pubmed ID | 23825009 | Accession Number(s) | nsv977903
| Frequency | Sample Size | 10 | Observed Gain | 10 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|
|