Variant DetailsVariant: nsv519771Internal ID | 15100378 | Landmark | | Location Information | | Cytoband | 9p24.1 | Allele length | Assembly | Allele length | hg38 | 3156 | hg19 | 3156 | hg18 | 3156 | hg17 | 3156 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv659183, nssv676309, nssv661704, nssv658438, nssv675996, nssv681109, nssv691639, nssv688016 | Samples | | Known Genes | CD274 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv519771
| Frequency | Sample Size | 2026 | Observed Gain | 0 | Observed Loss | 8 | Observed Complex | 0 | Frequency | n/a |
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