Variant DetailsVariant: dgv6933n100 Internal ID | 20158549 | Landmark | | Location Information | | Cytoband | 8p23.1 | Allele length | Assembly | Allele length | hg38 | 153073 | hg19 | 153073 | hg18 | 153073 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv1020003, nsv1025178, nsv1026653, nsv1025342, nsv1023797, nsv1020695, nsv1025968, nsv1022559, nsv1019645, nsv1021914, nsv1024098, nsv1032783, nsv1020563, nsv1021084, nsv1020629, nsv1021585, nsv1022997, nsv1028996, nsv1027633, nsv1020286, nsv1019076, nsv1029391, nsv1034479, nsv1024722, nsv1029810, nsv1015289, nsv1016590 | Samples | | Known Genes | DEFB103A, DEFB103B, DEFB104A, DEFB104B, DEFB105A, DEFB105B, DEFB106A, DEFB106B, DEFB107A, DEFB107B, DEFB4B, PRR23D1, PRR23D2, SPAG11B | 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) | dgv6933n100
| Frequency | Sample Size | 29084 | Observed Gain | 0 | Observed Loss | 33 | Observed Complex | 0 | Frequency | n/a |
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