Variant DetailsVariant: nsv1028324Internal ID | 18770855 | Landmark | | Location Information | | Cytoband | 8p23.1 | Allele length | Assembly | Allele length | hg38 | 165774 | hg19 | 165774 | hg18 | 165774 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv6961n100 | Supporting Variants | nssv3680847, nssv3680846, nssv3680836, nssv3680855, nssv3680851, nssv3680840, nssv3680842, nssv3680852, nssv3680839, nssv3680843, nssv3680849, nssv3680838, nssv3680854, nssv3680841, nssv3680856, nssv3680844, nssv3680837, nssv3680850, nssv3680845, nssv3680853, nssv3680848 | Samples | | Known Genes | DEFB103A, DEFB103B, DEFB104A, DEFB104B, DEFB105A, DEFB105B, DEFB106A, DEFB106B, DEFB107A, DEFB107B, DEFB4A, PRR23D1, PRR23D2, SPAG11A, SPAG11B, ZNF705B | 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) | nsv1028324
| Frequency | Sample Size | 29084 | Observed Gain | 8 | Observed Loss | 13 | Observed Complex | 0 | Frequency | n/a |
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