Variant DetailsVariant: nsv1051208 Internal ID | 18793739 | Landmark | | Location Information | | Cytoband | 15q14 | Allele length | Assembly | Allele length | hg38 | 105286 | hg19 | 105286 | hg18 | 105286 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv2558n100 | Supporting Variants | nssv3547911, nssv3721665, nssv3547907, nssv3721676, nssv3547908, nssv3548653, nssv3721666, nssv3548656, nssv3548650, nssv3548657, nssv3548654, nssv3548651, nssv3547905, nssv3721673, nssv3547902, nssv3548658, nssv3721672, nssv3721678, nssv3721674, nssv3721668, nssv3721677, nssv3721670, nssv3548652, nssv3721669, nssv3721675, nssv3721671, nssv3721679, nssv3548655, nssv3547903, nssv3721667, nssv3547904, nssv3547909, nssv3547906, nssv3547910 | 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) | nsv1051208
| Frequency | Sample Size | 29084 | Observed Gain | 4 | Observed Loss | 30 | Observed Complex | 0 | Frequency | n/a |
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