Variant DetailsVariant: nssv1175071Internal ID | 15531393 | Landmark | | Location Information | | Cytoband | 10q26.3 | Allele length | Assembly | Allele length | hg38 | 52437 | hg19 | 52437 | hg18 | 52437 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv552729 | Supporting Variants | | Samples | HGDP01091 | Known Genes | CYP2E1, SPRNP1, SYCE1 | 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) | nssv1175071
| Frequency | Sample Size | 17421 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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