Variant DetailsVariant: esv2731280Internal ID | 9965597 | Landmark | | Location Information | | Cytoband | 5q35.3 | Allele length | Assembly | Allele length | hg38 | 968 | hg19 | 968 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6911198, essv6934580, essv6887097, essv6854465, essv6824987, essv6974582, essv6943039, essv6947687, essv6911197, essv6759420, essv6926677 | Samples | SSM008, SSM024, SSM011, SSM021, SSM029, SSM019, SSM001, SSM015, SSM010, SSM012 | Known Genes | ADAMTS2 | Method | Sequencing | Analysis | Breakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads | Platform | Illumina HiSeq 2000 | Comments | | Reference | Wong_et_al_2012b | Pubmed ID | 23290073 | Accession Number(s) | esv2731280
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 10 | Observed Complex | 0 | Frequency | n/a |
|
|