Variant DetailsVariant: nsv517409Internal ID | 15098016 | Landmark | | Location Information | | Cytoband | 13q32.2 | Allele length | Assembly | Allele length | hg38 | 26362 | hg19 | 26362 | hg18 | 26362 | hg17 | 26362 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv701177, nssv696029, nssv659415, nssv675599, nssv651934, nssv679894, nssv655062, nssv694284, nssv689645, nssv688464, nssv668306 | Samples | | Known Genes | FARP1, STK24 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv517409
| Frequency | Sample Size | 2026 | Observed Gain | 1 | Observed Loss | 10 | Observed Complex | 0 | Frequency | n/a |
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