Variant DetailsVariant: nssv2763580Internal ID | 17537199 | Landmark | | Location Information | | Cytoband | 8p23.1 | Allele length | Assembly | Allele length | hg38 | 6331 | hg19 | 6331 | hg18 | 6331 |
| Variant Type | CNV deletion | Copy Number | 1 | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv972228 | Supporting Variants | | Samples | HGDP01307 | Known Genes | | Method | Sequencing | Analysis | Human CNVs | Platform | Not reported | Comments | | Reference | Sudmant_et_al_2013 | Pubmed ID | 23825009 | Accession Number(s) | nssv2763580
| Frequency | Sample Size | 10 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
|
|