Variant DetailsVariant: dgv7026n100Internal ID | 20158642 | Landmark | | Location Information | | Cytoband | 8p23.1 | Allele length | Assembly | Allele length | hg38 | 455330 | hg19 | 455330 | hg18 | 462292 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv1022418, nsv1030448, nsv1021732, nsv1017985, nsv1033009, nsv1017918, nsv1034930, nsv1026142, nsv1028351 | Samples | | Known Genes | DEFB109P1, DEFB130, FAM66A, FAM66D, FAM86B1, FAM86B2, FAM90A25P, FAM90A2P, LOC100133267, LOC100506990, LOC649352, LOC729732, USP17L2, USP17L7 | 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) | dgv7026n100
| Frequency | Sample Size | 29084 | Observed Gain | 66 | Observed Loss | 21 | Observed Complex | 0 | Frequency | n/a |
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