Variant DetailsVariant: esv2727527 Internal ID | 9961837 | Landmark | | Location Information | | Cytoband | 4p12 | Allele length | Assembly | Allele length | hg38 | 1180 | hg19 | 1180 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6918222, essv6934142, essv6910830, essv6848272, essv6693635, essv6791010, essv6711361, essv6926357, essv6789965, essv6922572, essv6715017, essv6667276, essv6670240, essv6973823, essv6774164, essv6938472, essv6785855, essv6840743, essv6755687, essv6903236, essv6942728, essv6947291, essv6770306, essv6675977 | Samples | SSM065, SSM022, SSM013, SSM086, SSM084, SSM042, SSM043, SSM031, SSM032, SSM024, SSM017, SSM009, SSM066, SSM029, SSM030, SSM069, SSM021, SSM037, SSM019, SSM023, SSM015, SSM008, SSM018, SSM070 | Known Genes | ATP10D | 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) | esv2727527
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 24 | Observed Complex | 0 | Frequency | n/a |
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