Internal ID | 18837363 |
Landmark | |
Location Information | |
Cytoband | 19q13.32 |
Allele length | Assembly | Allele length | hg38 | 22537 | hg19 | 22537 | hg18 | 22537 |
|
Variant Type | CNV loss |
Copy Number | |
Allele State | |
Allele Origin | |
Probe Count | |
Validation Flag | |
Merged Status | M |
Merged Variants | |
Supporting Variants | essv25798042 |
Samples | |
Known Genes | SYNGR4, TMEM143 |
Method | SNP array |
Analysis | |
Platform | Illumina Human OmniExpress |
Comments | |
Reference | Suktitipat_et_al_2014 |
Pubmed ID | 25118596 |
Accession Number(s) | esv3893229
|
Frequency | Sample Size | 3017 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
|