Internal ID | 20139613 |
Landmark | |
Location Information | |
Cytoband | 19p13.3 |
Allele length | Assembly | Allele length | hg38 | 964 | hg19 | 964 | hg18 | 964 |
|
Variant Type | CNV gain+loss |
Copy Number | |
Allele State | |
Allele Origin | |
Probe Count | |
Validation Flag | |
Merged Status | M |
Merged Variants | |
Supporting Variants | nsv578230, nsv578237, nsv578229, nsv578246 |
Samples | |
Known Genes | SBNO2 |
Method | SNP array |
Analysis | Illumina SNP array copy number analysis |
Platform | Not reported |
Comments | |
Reference | Cooper_et_al_2011 |
Pubmed ID | 21841781 |
Accession Number(s) | dgv6189n54
|
Frequency | Sample Size | 17421 | Observed Gain | 67 | Observed Loss | 21 | Observed Complex | 0 | Frequency | n/a |
|