Variant DetailsVariant: dgv3248n100Internal ID | 20154864 | Landmark | | Location Information | | Cytoband | 17q21.31 | Allele length | Assembly | Allele length | hg38 | 328817 | hg19 | 328817 | hg18 | 328356 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv1058499, nsv1057064, nsv1065393, nsv1062988, nsv1058752, nsv1055434, nsv1056215, nsv1064352, nsv1056925, nsv1066703, nsv1057050, nsv1063729, nsv1057394 | Samples | | Known Genes | ARL17A, ARL17B, 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) | dgv3248n100
| Frequency | Sample Size | 29084 | Observed Gain | 0 | Observed Loss | 21 | Observed Complex | 0 | Frequency | n/a |
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