| Internal ID | 15039059 |
| Landmark | |
| Location Information | |
| Cytoband | Xq25 |
| Allele length | | Assembly | Allele length | | hg38 | 707 | | hg19 | 707 | | hg18 | 707 | | hg16 | 707 |
|
| Variant Type | CNV loss |
| Copy Number | |
| Allele State | |
| Allele Origin | |
| Probe Count | |
| Validation Flag | |
| Merged Status | S |
| Merged Variants | nsv438155 |
| Supporting Variants | |
| Samples | NA18540 |
| Known Genes | STAG2 |
| 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) | nssv470221
|
| Frequency | | Sample Size | 269 | | Observed Gain | 0 | | Observed Loss | 1 | | Observed Complex | 0 | | Frequency | n/a |
|
