Internal ID | 6676969 |
Landmark | |
Location Information | |
Cytoband | 15q23 |
Allele length | Assembly | Allele length | hg38 | 11131 | hg19 | 11131 |
|
Variant Type | CNV loss |
Copy Number | |
Allele State | |
Allele Origin | |
Probe Count | |
Validation Flag | |
Merged Status | M |
Merged Variants | |
Supporting Variants | essv15287959, essv15287960, essv15287961 |
Samples | HG00632, HG02082, HG00864 |
Known Genes | THSD4 |
Method | Sequencing |
Analysis | |
Platform | Multiple platforms |
Comments | |
Reference | 1000_Genomes_Consortium_Phase_3 |
Pubmed ID | 21293372 |
Accession Number(s) | esv3636862
|
Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 3 | Observed Complex | 0 | Frequency | n/a |
|