Internal ID | 20139704 |
Landmark | |
Location Information | |
Cytoband | 19p13.12 |
Allele length | Assembly | Allele length | hg38 | 1123 | hg19 | 1123 | hg18 | 1123 |
|
Variant Type | CNV loss |
Copy Number | |
Allele State | |
Allele Origin | |
Probe Count | |
Validation Flag | |
Merged Status | M |
Merged Variants | |
Supporting Variants | nsv578671, nsv578670, nsv578669, nsv578668 |
Samples | |
Known Genes | EMR3 |
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) | dgv6280n54
|
Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 6 | Observed Complex | 0 | Frequency | n/a |
|