Variant DetailsVariant: nsv1006838Internal ID | 18749369 | Landmark | | Location Information | | Cytoband | 1q21.2 | Allele length | Assembly | Allele length | hg38 | 296843 | hg19 | 296843 | hg18 | 296843 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv3491726 | Samples | | Known Genes | ADAMTSL4, ADAMTSL4-AS1, CTSS, ECM1, ENSA, GOLPH3L, HORMAD1, LINC00568, MCL1, MIR4257, MIR6878, RPRD2, TARS2 | 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) | nsv1006838
| Frequency | Sample Size | 29084 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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