Variant DetailsVariant: nsv1039585Internal ID | 18782116 | Landmark | | Location Information | | Cytoband | 15q14 | Allele length | Assembly | Allele length | hg38 | 119221 | hg19 | 119221 | hg18 | 119221 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv2558n100 | Supporting Variants | nssv3721691, nssv3548687, nssv3721693, nssv3548679, nssv3548670, nssv3548688, nssv3548684, nssv3548678, nssv3721683, nssv3721688, nssv3548676, nssv3548677, nssv3721684, nssv3721692, nssv3548674, nssv3721690, nssv3548682, nssv3548671, nssv3721686, nssv3548672, nssv3548673, nssv3548680, nssv3721689, nssv3548681, nssv3548686, nssv3548683, nssv3721687, nssv3548685, nssv3548669, nssv3548675, nssv3721685 | 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) | nsv1039585
| Frequency | Sample Size | 29084 | Observed Gain | 4 | Observed Loss | 27 | Observed Complex | 0 | Frequency | n/a |
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