Variant DetailsVariant: essv13451378Internal ID | 3453194 | Landmark | | Location Information | | Cytoband | 9p21.1 | Allele length | Assembly | Allele length | hg38 | 500332 | hg19 | 500332 |
| Variant Type | CNV gain | Copy Number | | Allele State | Heterozygous | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | esv3620303 | Supporting Variants | | Samples | HG01602 | Known Genes | APTX, DNAJA1, NDUFB6, SMU1, TAF1L, TMEM215 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | essv13451378
| Frequency | Sample Size | 2504 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|
|