Variant DetailsVariant: nsv1054353Internal ID | 18796884 | Landmark | | Location Information | | Cytoband | 15q14 | Allele length | Assembly | Allele length | hg38 | 160497 | hg19 | 160497 | hg18 | 160497 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv2559n100 | Supporting Variants | nssv3548760, nssv3548751, nssv3548763, nssv3548757, nssv3548762, nssv3548764, nssv3548752, nssv3721715, nssv3721713, nssv3548761, nssv3548750, nssv3721718, nssv3548753, nssv3548758, nssv3721717, nssv3548754, nssv3548755, nssv3548759, nssv3721716, nssv3721720, nssv3721714, nssv3721719, nssv3548756 | Samples | | Known Genes | GOLGA8A, 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) | nsv1054353
| Frequency | Sample Size | 29084 | Observed Gain | 3 | Observed Loss | 20 | Observed Complex | 0 | Frequency | n/a |
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