Variant DetailsVariant: nsv1066676Internal ID | 18809207 | Landmark | | Location Information | | Cytoband | 17p13.3 | Allele length | Assembly | Allele length | hg38 | 136451 | hg19 | 136451 | hg18 | 136451 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv3074n100 | Supporting Variants | nssv3560047, nssv3560046 | Samples | | Known Genes | DBIL5P, FAM57A, GEMIN4, GLOD4, NXN, RNMTL1 | 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) | nsv1066676
| Frequency | Sample Size | 29084 | Observed Gain | 2 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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