Variant DetailsVariant: nsv1047892Internal ID | 18790423 | Landmark | | Location Information | | Cytoband | 15q14 | Allele length | Assembly | Allele length | hg38 | 91073 | hg19 | 91073 | hg18 | 91073 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv2569n100 | Supporting Variants | nssv3551719, nssv3551713, nssv3551722, nssv3551714, nssv3551710, nssv3552096, nssv3551712, nssv3552093, nssv3551716, nssv3551721, nssv3551708, nssv3551718, nssv3551709, nssv3552095, nssv3716654, nssv3552094, nssv3551720, nssv3551715, nssv3551711, nssv3551717, nssv3551723 | Samples | | Known Genes | GOLGA8B, MIR1233-1, MIR1233-2 | 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) | nsv1047892
| Frequency | Sample Size | 29084 | Observed Gain | 0 | Observed Loss | 21 | Observed Complex | 0 | Frequency | n/a |
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