Variant DetailsVariant: nsv517777Internal ID | 15098384 | Landmark | | Location Information | | Cytoband | 3p14.2 | Allele length | Assembly | Allele length | hg38 | 3008 | hg19 | 3008 | hg18 | 3008 | hg17 | 3008 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv653213, nssv669514, nssv656981, nssv687616, nssv689402, nssv677536, nssv675265, nssv677925, nssv654481, nssv665364, nssv686453, nssv692614, nssv663131, nssv664317, nssv696588, nssv666521, nssv698604, nssv693384, nssv656406, nssv680487, nssv659755, nssv678197, nssv670168, nssv661022, nssv677875, nssv658129, nssv692332 | Samples | | Known Genes | CADPS | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv517777
| Frequency | Sample Size | 2026 | Observed Gain | 0 | Observed Loss | 27 | Observed Complex | 0 | Frequency | n/a |
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