Variant DetailsVariant: dgv1355n54Internal ID | 20134779 | Landmark | | Location Information | | Cytoband | 10q23.33 | Allele length | Assembly | Allele length | hg38 | 246123 | hg19 | 246123 | hg18 | 246123 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv551956, nsv551955, nsv551957 | Samples | | Known Genes | CYP2C18, CYP2C19 | Method | SNP array | Analysis | Illumina SNP array copy number analysis | Platform | Not reported | Comments | | Reference | Cooper_et_al_2011 | Pubmed ID | 21841781 | Accession Number(s) | dgv1355n54
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 3 | Observed Complex | 0 | Frequency | n/a |
|
|