Variant DetailsVariant: nsv615209Internal ID | 16055932 | Landmark | | Location Information | | Cytoband | 9q32 | Allele length | Assembly | Allele length | hg38 | 14562 | hg19 | 14562 | hg18 | 14562 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv1176130, nssv1176134, nssv1176135, nssv1141251, nssv1176128, nssv1176137, nssv1176131, nssv1176129, nssv1141252, nssv1141250, nssv1176132, nssv1176136, nssv1176133, nssv1141253, nssv1141254 | Samples | HGDP00216, HGDP00920, HGDP00931, HGDP00906, HGDP00160, HGDP01094, HGDP00057, HGDP00918, HGDP00681, HGDP00454 | Known Genes | FAM225B | Method | SNP array | Analysis | Illumina SNP array copy number analysis | Platform | Not reported | Comments | | Reference | Cooper_et_al_2011 | Pubmed ID | 21841781 | Accession Number(s) | nsv615209
| Frequency | Sample Size | 17421 | Observed Gain | 1 | Observed Loss | 14 | Observed Complex | 0 | Frequency | n/a |
|
|