Internal ID | 6675408 |
Landmark | |
Location Information | |
Cytoband | 14q32.11 |
Allele length | Assembly | Allele length | hg38 | 9859 | hg19 | 9859 |
|
Variant Type | CNV loss |
Copy Number | |
Allele State | |
Allele Origin | |
Probe Count | |
Validation Flag | |
Merged Status | M |
Merged Variants | |
Supporting Variants | essv15093033, essv15093032, essv15093034 |
Samples | HG00236, NA20811, NA20818 |
Known Genes | FOXN3 |
Method | Sequencing |
Analysis | |
Platform | Multiple platforms |
Comments | |
Reference | 1000_Genomes_Consortium_Phase_3 |
Pubmed ID | 21293372 |
Accession Number(s) | esv3635295
|
Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 3 | Observed Complex | 0 | Frequency | n/a |
|