Internal ID | 9579269 |
Landmark | |
Location Information | |
Cytoband | 7p15.2 |
Allele length | Assembly | Allele length | hg38 | 954 | hg19 | 954 |
|
Variant Type | CNV deletion |
Copy Number | |
Allele State | |
Allele Origin | |
Probe Count | |
Validation Flag | |
Merged Status | M |
Merged Variants | |
Supporting Variants | essv5665914, essv6413572, essv5817629, essv6003083 |
Samples | NA18627, HG00543, NA18541, NA18549 |
Known Genes | NFE2L3 |
Method | Merging |
Analysis | No reference, merging analysis |
Platform | Merging |
Comments | High quality site |
Reference | 1000_Genomes_Consortium_Phase_1 |
Pubmed ID | 23128226 |
Accession Number(s) | esv2659850
|
Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 4 | Observed Complex | 0 | Frequency | n/a |
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