Internal ID | 14697563 |
Landmark | |
Location Information | |
Cytoband | 11q13.1 |
Allele length | Assembly | Allele length | hg38 | 2999 | hg19 | 2999 | hg18 | 2999 |
|
Variant Type | CNV duplication |
Copy Number | |
Allele State | |
Allele Origin | |
Probe Count | |
Validation Flag | |
Merged Status | S |
Merged Variants | esv3361899 |
Supporting Variants | |
Samples | NA19239 |
Known Genes | CLCF1, LOC100130987 |
Method | Sequencing |
Analysis | |
Platform | Illumina |
Comments | |
Reference | 1000_Genomes_Consortium_Pilot_Project |
Pubmed ID | 20981092 |
Accession Number(s) | essv8688494
|
Frequency | Sample Size | 185 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|