Variant DetailsVariant: nsv437864Internal ID | 15041095 | Landmark | | Location Information | | Cytoband | 3p14.1 | Allele length | Assembly | Allele length | hg38 | 2025 | hg19 | 2025 | hg18 | 2025 | hg16 | 2025 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv471282, nssv471283 | Samples | NA18967, NA18940 | Known Genes | FAM19A1 | 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) | nsv437864
| Frequency | Sample Size | 269 | Observed Gain | 0 | Observed Loss | 2 | Observed Complex | 0 | Frequency | n/a |
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