Internal ID | 20150027 |
Landmark | |
Location Information | |
Cytoband | 5p15.31 |
Allele length | Assembly | Allele length | hg38 | 2687 | hg19 | 2687 |
|
Variant Type | CNV loss |
Copy Number | |
Allele State | |
Allele Origin | |
Probe Count | |
Validation Flag | |
Merged Status | M |
Merged Variants | |
Supporting Variants | esv3569936, esv3569938, esv3569937 |
Samples | 401146US, 401842BJ, 401494PD, 401166WJ, 400645KM |
Known Genes | SRD5A1 |
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) | dgv1571e212
|
Frequency | Sample Size | 873 | Observed Gain | 0 | Observed Loss | 5 | Observed Complex | 0 | Frequency | n/a |
|