Internal ID | 9534903 |
Landmark | |
Location Information | |
Cytoband | 17p11.1 |
Allele length | Assembly | Allele length | hg38 | 1058957 | hg19 | 658170 |
|
Variant Type | CNV deletion |
Copy Number | |
Allele State | |
Allele Origin | |
Probe Count | |
Validation Flag | 1 |
Merged Status | S |
Merged Variants | esv2676591 |
Supporting Variants | |
Samples | HG01082 |
Known Genes | FAM27L, FLJ36000, MTRNR2L1 |
Method | Merging |
Analysis | No reference, merging analysis |
Platform | Merging |
Comments | |
Reference | 1000_Genomes_Consortium_Phase_1 |
Pubmed ID | 23128226 |
Accession Number(s) | essv6557500
|
Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
|