Variant DetailsVariant: nsv1043647Internal ID | 18786178 | Landmark | | Location Information | | Cytoband | 15q13.2 | Allele length | Assembly | Allele length | hg38 | 153294 | hg19 | 153294 | hg18 | 153294 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv2519n100 | Supporting Variants | nssv3547565, nssv3547566, nssv3721566, nssv3547564, nssv3547561, nssv3547562, nssv3547563 | Samples | | Known Genes | CHRFAM7A, LOC101059918 | 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) | nsv1043647
| Frequency | Sample Size | 29084 | Observed Gain | 0 | Observed Loss | 7 | Observed Complex | 0 | Frequency | n/a |
|
|