Variant DetailsVariant: dgv2118e212![](http://dgv.tcag.ca/gb2/gbrowse_img/dgv2_hg38/?name=chr8:143616751..143643564;width=800;overview=1) Internal ID | 20150574 | Landmark | | Location Information | | Cytoband | 8q24.3 | Allele length | Assembly | Allele length | hg38 | 26814 | hg19 | 26814 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | esv3573035, esv3573034, esv3573033 | Samples | 401956DQ, 401733CG, 400155CW, 401303FM, 401406KF, 400844GP, 400719TM, 401480PG | Known Genes | TSTA3, ZNF623 | Method | SNP array | Analysis | We used four separate algorithms to detect CNVs; Affymetrix Chromosome Analysis Suite (ChAS), iPattern, Nexus and Partek. Our primary analysis was performed based on ChAS CNV calls, which were then supported using the remaining three algorithms to construct a confidence set of CNVs. For all algorithms, we have used 8 probes and >1kb as a base line cutoff for CNV detection. | Platform | Affymetrix CytoScan HD 2.7M array | Comments | | Reference | Uddin_et_al_2014 | Pubmed ID | 25503493 | Accession Number(s) | dgv2118e212
| Frequency | Sample Size | 873 | Observed Gain | 0 | Observed Loss | 8 | Observed Complex | 0 | Frequency | n/a |
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