Variant DetailsVariant: nsv1058939Internal ID | 18801470 | Landmark | | Location Information | | Cytoband | 17q21.31 | Allele length | Assembly | Allele length | hg38 | 539085 | hg19 | 539085 | hg18 | 538487 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv3196n100 | Supporting Variants | nssv3550120, nssv3550110, nssv3550112, nssv3550118, nssv3550130, nssv3550127, nssv3550121, nssv3550113, nssv3550116, nssv3723873, nssv3550128, nssv3723871, nssv3550124, nssv3550123, nssv3550129, nssv3550114, nssv3550126, nssv3550125, nssv3550117, nssv3723872, nssv3550122, nssv3550119, nssv3550115, nssv3550111 | Samples | | Known Genes | ARL17A, ARL17B, KANSL1, KANSL1-AS1, LOC644172, LRRC37A, LRRC37A2, NSF, NSFP1 | 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) | nsv1058939
| Frequency | Sample Size | 29084 | Observed Gain | 14 | Observed Loss | 10 | Observed Complex | 0 | Frequency | n/a |
|
|