Variant DetailsVariant: dgv2347n100Internal ID | 19012715 | Landmark | | Location Information | | Cytoband | 15q11.2 | Allele length | Assembly | Allele length | hg38 | 1227055 | hg19 | 1309677 | hg18 | 546383 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv1038878, nsv1050913, nsv1041600, nsv1045393, nsv1048242, nsv1035318, nsv1040743, nsv1038054, nsv1050173, nsv1035417, nsv1044204, nsv1048271, nsv1038828, nsv1045707, nsv1045125, nsv1054420, nsv1040146 | Samples | | Known Genes | CT60, CXADRP2, LOC646214, LOC727924, NF1P2, OR4M2, OR4N4, POTEB, POTEB2 | 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) | dgv2347n100
| Frequency | Sample Size | 29084 | Observed Gain | 0 | Observed Loss | 21 | Observed Complex | 0 | Frequency | n/a |
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