Variant DetailsVariant: esv3639191Internal ID | 6679286 | Landmark | | Location Information | | Cytoband | 16q23.1 | Allele length | Assembly | Allele length | hg38 | 25169 | hg19 | 25169 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv539e214 | Supporting Variants | essv15528514, essv15528513 | Samples | HG03100, HG02489 | Known Genes | WWOX | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3639191
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 2 | Observed Complex | 0 | Frequency | n/a |
|
|