Internal ID | 6628779 |
Landmark | |
Location Information | |
Cytoband | 1q31.3 |
Allele length | Assembly | Allele length | hg38 | 24677 | hg19 | 24677 |
|
Variant Type | CNV loss |
Copy Number | |
Allele State | |
Allele Origin | |
Probe Count | |
Validation Flag | |
Merged Status | M |
Merged Variants | dgv72e214 |
Supporting Variants | essv10253769, essv10253770, essv10253768 |
Samples | HG02870, NA19200, HG02449 |
Known Genes | CFHR5 |
Method | Sequencing |
Analysis | |
Platform | Multiple platforms |
Comments | |
Reference | 1000_Genomes_Consortium_Phase_3 |
Pubmed ID | 21293372 |
Accession Number(s) | esv3588487
|
Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 3 | Observed Complex | 0 | Frequency | n/a |
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