Variant DetailsVariant: nsv437902Internal ID | 15041133 | Landmark | | Location Information | | Cytoband | 3q28 | Allele length | Assembly | Allele length | hg38 | 3556 | hg19 | 3556 | hg18 | 3556 | hg16 | 3556 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv467893, nssv467889, nssv467892, nssv467891, nssv467884, nssv467890, nssv467885, nssv467888, nssv467887 | Samples | NA18504, NA18944, NA18547, NA18949, NA18503, NA18570, NA19211, NA18609, NA18612 | Known Genes | TP63 | Method | SNP array | Analysis | Null genotypes - for each genotype assay and population sample we defined the null genotype pattern of that assay as the binary vector (length 90) of null genotype calls across the 90 individuals. | Platform | Not reported | Comments | | Reference | McCarroll_et_al_2006 | Pubmed ID | 16468122 | Accession Number(s) | nsv437902
| Frequency | Sample Size | 269 | Observed Gain | 0 | Observed Loss | 9 | Observed Complex | 0 | Frequency | n/a |
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