Variant DetailsVariant: nsv1035788Internal ID | 18778319 | Landmark | | Location Information | | Cytoband | 15q14 | Allele length | Assembly | Allele length | hg38 | 99925 | hg19 | 99925 | hg18 | 99925 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv2558n100 | Supporting Variants | nssv3548855, nssv3548853, nssv3721737, nssv3721738, nssv3548854, nssv3548850, nssv3548852, nssv3721736, nssv3721735, nssv3548856, nssv3548851 | 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) | nsv1035788
| Frequency | Sample Size | 29084 | Observed Gain | 2 | Observed Loss | 9 | Observed Complex | 0 | Frequency | n/a |
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