Variant DetailsVariant: nsv1015978Internal ID | 18758513 | Landmark | | Location Information | | Cytoband | 8p23.1 | Allele length | Assembly | Allele length | hg38 | 509807 | hg19 | 509807 | hg18 | 559807 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv6936n100 | Supporting Variants | nssv3679822, nssv3679820, nssv3756401, nssv3679818, nssv3679817, nssv3679819, nssv3679821, nssv3679824, nssv3679826, nssv3679823, nssv3679825 | Samples | | Known Genes | DEFB103A, DEFB103B, DEFB104A, DEFB104B, DEFB105A, DEFB105B, DEFB106A, DEFB106B, DEFB107A, DEFB107B, DEFB4A, DEFB4B, FAM90A10P, FAM90A7P, PRR23D1, PRR23D2, SPAG11A, 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) | nsv1015978
| Frequency | Sample Size | 29084 | Observed Gain | 4 | Observed Loss | 7 | Observed Complex | 0 | Frequency | n/a |
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