Variant DetailsVariant: nsv516886Internal ID | 15097493 | Landmark | | Location Information | | Cytoband | 17p13.3 | Allele length | Assembly | Allele length | hg38 | 45455 | hg19 | 45455 | hg18 | 45455 | hg17 | 45455 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv692260, nssv679402, nssv682227, nssv672239, nssv654693 | Samples | | Known Genes | MIR22, MIR22HG, SERPINF2, TLCD2, WDR81 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv516886
| Frequency | Sample Size | 2026 | Observed Gain | 0 | Observed Loss | 5 | Observed Complex | 0 | Frequency | n/a |
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