Variant DetailsVariant: esv3638931Internal ID | 6679028 | Landmark | | Location Information | | Cytoband | 16q22.1 | Allele length | Assembly | Allele length | hg38 | 61494 | hg19 | 61494 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv15503750 | Samples | HG02079 | Known Genes | NOB1, WWP2 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3638931
| Frequency | Sample Size | 2504 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|
|