Internal ID | 15997318 |
Landmark | |
Location Information | |
Cytoband | 11q25 |
Allele length | Assembly | Allele length | hg38 | 24696 | hg19 | 24696 | hg18 | 24696 |
|
Variant Type | CNV loss |
Copy Number | |
Allele State | |
Allele Origin | |
Probe Count | |
Validation Flag | |
Merged Status | M |
Merged Variants | |
Supporting Variants | nssv1176205 |
Samples | HGDP00976 |
Known Genes | IGSF9B, MIR4697, MIR4697HG |
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) | nsv556595
|
Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
|