Variant DetailsVariant: nsv515681Internal ID | 15096288 | Landmark | | Location Information | | Cytoband | 19q13.32 | Allele length | Assembly | Allele length | hg38 | 11116 | hg19 | 11116 | hg18 | 11116 | hg17 | 11116 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv675988, nssv664367, nssv686357 | Samples | | Known Genes | ERCC2 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv515681
| Frequency | Sample Size | 2026 | Observed Gain | 0 | Observed Loss | 3 | Observed Complex | 0 | Frequency | n/a |
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