Internal ID | 8978290 |
Landmark | |
Location Information | |
Cytoband | 12q23.3 |
Allele length | Assembly | Allele length | hg38 | 3248 | hg19 | 3248 |
|
Variant Type | CNV deletion |
Copy Number | |
Allele State | |
Allele Origin | |
Probe Count | |
Validation Flag | 1 |
Merged Status | S |
Merged Variants | esv2661506 |
Supporting Variants | |
Samples | HG01079 |
Known Genes | CHST11 |
Method | Merging |
Analysis | No reference, merging analysis |
Platform | Merging |
Comments | |
Reference | 1000_Genomes_Consortium_Phase_1 |
Pubmed ID | 23128226 |
Accession Number(s) | essv6000887
|
Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
|