Variant DetailsVariant: nsv1007615Internal ID | 18750146 | Landmark | | Location Information | | Cytoband | 1p36.11 | Allele length | Assembly | Allele length | hg38 | 65555 | hg19 | 65555 | hg18 | 65555 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv137n100 | Supporting Variants | nssv3470240, nssv3476683, nssv3466647, nssv3698493, nssv3466531, nssv3698494, nssv3474706 | Samples | | Known Genes | RHD | Method | SNP array | Analysis | Affymetrix SNP array copy number analysis | Platform | Affymetrix SNP Array 6.0 | Comments | | Reference | Coe_et_al_2014 | Pubmed ID | 25217958 | Accession Number(s) | nsv1007615
| Frequency | Sample Size | 29084 | Observed Gain | 2 | Observed Loss | 5 | Observed Complex | 0 | Frequency | n/a |
|
|