Variant DetailsVariant: nsv521589Internal ID | 15102196 | Landmark | | Location Information | | Cytoband | 7p22.1 | Allele length | Assembly | Allele length | hg38 | 119998 | hg19 | 119998 | hg18 | 119998 | hg17 | 119998 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv402n21 | Supporting Variants | nssv698207 | Samples | | Known Genes | OCM, RNF216, ZNF815P | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv521589
| Frequency | Sample Size | 2026 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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