Variant DetailsVariant: esv3624256Internal ID | 6664423 | Landmark | | Location Information | | Cytoband | 10q23.33 | Allele length | Assembly | Allele length | hg38 | 44223 | hg19 | 44223 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv13902091, essv13902092 | Samples | HG00185, HG00268 | Known Genes | CYP2C18, CYP2C19 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3624256
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 2 | Observed Complex | 0 | Frequency | n/a |
|
|