Internal ID | 16026657 |
Landmark | |
Location Information | |
Cytoband | 20q11.22 |
Allele length | Assembly | Allele length | hg38 | 1331 | hg19 | 1331 | hg18 | 1331 |
|
Variant Type | CNV loss |
Copy Number | |
Allele State | |
Allele Origin | |
Probe Count | |
Validation Flag | |
Merged Status | M |
Merged Variants | dgv7561n54 |
Supporting Variants | nssv939313, nssv939312, nssv939314, nssv939311 |
Samples | |
Known Genes | PIGU |
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) | nsv585934
|
Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 4 | Observed Complex | 0 | Frequency | n/a |
|