Variant DetailsVariant: nsv519767Internal ID | 15100374 | Landmark | | Location Information | | Cytoband | 9q33.3 | Allele length | Assembly | Allele length | hg38 | 116911 | hg19 | 116911 | hg18 | 116911 | hg17 | 116911 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv692234, nssv688352, nssv658400, nssv685856, nssv660877, nssv679769, nssv674014, nssv683298, nssv683358 | Samples | | Known Genes | LOC100129034, NEK6, PSMB7 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv519767
| Frequency | Sample Size | 2026 | Observed Gain | 0 | Observed Loss | 9 | Observed Complex | 0 | Frequency | n/a |
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