Variant DetailsVariant: esv2749610Internal ID | 9983894 | Landmark | | Location Information | | Cytoband | 15q15.1 | Allele length | Assembly | Allele length | hg38 | 1221 | hg19 | 1221 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6788164, essv6842847, essv6911217, essv6873974, essv6741309, essv6932280, essv6835244, essv6824018, essv6831703 | Samples | SSM079, SSM002, SSM084, SSM069, SSM081, SSM082, SSM020, SSM007, SSM091 | Known Genes | TYRO3 | 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) | esv2749610
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 9 | Observed Complex | 0 | Frequency | n/a |
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