Internal ID | 20143156 |
Landmark | |
Location Information | |
Cytoband | 5p12 |
Allele length | Assembly | Allele length | hg38 | 1684 | hg19 | 1684 | hg18 | 1684 |
|
Variant Type | CNV loss |
Copy Number | |
Allele State | |
Allele Origin | |
Probe Count | |
Validation Flag | |
Merged Status | M |
Merged Variants | |
Supporting Variants | nsv597889, nsv597890, nsv597891, nsv597888 |
Samples | |
Known Genes | GHR |
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) | dgv9732n54
|
Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 7 | Observed Complex | 0 | Frequency | n/a |
|