Internal ID | 15156138 |
Landmark | |
Location Information | |
Cytoband | 17q12 |
Allele length | Assembly | Allele length | hg38 | 25197 | hg19 | 25219 | hg18 | 25219 | hg17 | 25219 |
|
Variant Type | CNV gain |
Copy Number | 3 |
Allele State | |
Allele Origin | |
Probe Count | |
Validation Flag | |
Merged Status | S |
Merged Variants | nsv457736 |
Supporting Variants | |
Samples | 1780854556_A |
Known Genes | |
Method | SNP array |
Analysis | An HMM examining LogR Ratio and B-allele Frequency was used to classify SNP array data into regions of copy-number 0-3. A combination of manual and automated curation was used on the resulting output to reduce false positives. |
Platform | Not reported |
Comments | |
Reference | Itsara_et_al_2009 |
Pubmed ID | 19166990 |
Accession Number(s) | nssv534862
|
Frequency | Sample Size | 1557 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|