Variant DetailsVariant: nsv1046628Internal ID | 18789159 | Landmark | | Location Information | | Cytoband | 15q14 | Allele length | Assembly | Allele length | hg38 | 113860 | hg19 | 113860 | hg18 | 113860 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv2558n100 | Supporting Variants | nssv3548868, nssv3548875, nssv3548867, nssv3721740, nssv3548870, nssv3548869, nssv3548871, nssv3721746, nssv3548878, nssv3721742, nssv3721741, nssv3548877, nssv3721745, nssv3548872, nssv3721747, nssv3548876, nssv3721743, nssv3548874, nssv3721744, nssv3548873 | Samples | | Known Genes | GOLGA8A | 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) | nsv1046628
| Frequency | Sample Size | 29084 | Observed Gain | 2 | Observed Loss | 18 | Observed Complex | 0 | Frequency | n/a |
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