Variant DetailsVariant: nsv1062635Internal ID | 18805166 | Landmark | | Location Information | | Cytoband | 20q13.2 | Allele length | Assembly | Allele length | hg38 | 10092 | hg19 | 10092 | hg18 | 10092 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv4330n100 | Supporting Variants | nssv3587567, nssv3587565, nssv3587563, nssv3587566, nssv3587564 | Samples | | Known Genes | BCAS1 | 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) | nsv1062635
| Frequency | Sample Size | 29084 | Observed Gain | 0 | Observed Loss | 5 | Observed Complex | 0 | Frequency | n/a |
|
|