Hs03336984_cn

• Assay Reference Genome Location: Chr.1:634904 on build GRCh38
• Cytoband: 1p36.33

Target Copy Number Variation Details

• DGV Version: Release date: 2016-05-15, GRCh GRCh38

Target Variation	Location	CNV Subtype	Genes
nsv1004962	Chr.1:629241 - 915295 on Build GRCh38	Gain	OR4F16 LOC107984841 FAM87B LINC01128 MTND2P28 MTND1P23 MIR6723 LINC00115 LOC284600 LOC100287934 FAM41C LOC100133331 LOC100288069
dgv1e24	Chr.1:629054 - 714367 on Build GRCh38	Loss	MTND2P28 OR4F16 MTND1P23 MIR6723
nsv471522	Chr.1:586759 - 821403 on Build GRCh38	Gain	MTND2P28 OR4F16 MTND1P23 MIR6723 LOC101928626 LOC107984841 FAM87B LOC100287934 LOC105378947 LOC100133331 LOC100288069
nsv482937	Chr.1:10001 - 2368561 on Build GRCh38	Loss	SSU72 OR4F29 MIR1302-2 CDK11B LOC100288175 GABRD MIR6808 LINC01342 MTND1P23 LINC00115 LOC101928626 LOC107985728 AGRN MXRA8 FAM87B FAM132A SLC35E2 CALML6 LOC105378591 TMEM88B MIB2 LOC102724312 MIR200B MTND2P28 CPSF3L ISG15 SCNN1D SKI MIR6859-2 FAAP20 GNB1 MRPL20 TMEM240 LOC100130417 NADK FNDC10 FAM41C LOC105378947 LOC100288069 LOC148413 PLEKHN1 ATAD3C SAMD11 SLC35E2B CFAP74 B3GALT6 TTLL10-AS1 LOC729737 LOC105378948 TAS1R3 C1orf159 PUSL1 NOC2L CCNL2 CPTP UBE2J2 DDX11L1 LOC100134822 CDK11A TTLL10 MIR6859-1 LOC107984841 LOC107985729 LOC105378589 SDF4 VWA1 LOC100129534 MORN1 AURKAIP1 TNFRSF4 LOC100133331 OR4F16 KLHL17 PERM1 RNF223 MIR200A ATAD3B MIR429 LINC01128 MIR6723 MIR6726 LOC284600 MIR6727 HES4 LOC105378592 PRKCZ LOC105378949 MMP23B OR4F5 WASH7P FAM138A MMP23A DVL1 ATAD3A ANKRD65 ACAP3 LOC100132287 LOC100506504 LOC100287934 TNFRSF18 TMEM52 LOC102725121
nsv949752	Chr.1:628921 - 634920 on Build GRCh38	Duplication	MTND2P28 MTND1P23 MIR6723 LOC101928626
nsv1077276	Chr.1:629119 - 635620 on Build GRCh38	Duplication	MTND2P28 MTND1P23 MIR6723
esv3417080	Chr.1:629009 - 635007 on Build GRCh38	Duplication	MTND2P28 MTND1P23 MIR6723 LOC101928626
dgv5n100	Chr.1:585989 - 1114424 on Build GRCh38	Gain	OR4F16 KLHL17 PERM1 RNF223 LOC100288175 LINC01128 MTND1P23 MIR6723 LINC00115 LOC100130417 LOC101928626 LOC284600 FAM41C LOC107985728 AGRN LOC105378947 LOC100288069 HES4 PLEKHN1 SAMD11 LOC107984841 FAM87B LOC105378948 MTND2P28 ISG15 C1orf159 LOC100287934 NOC2L LOC100133331
nsv830758	Chr.1:603875 - 721370 on Build GRCh38	Loss	MTND2P28 OR4F16 MTND1P23 MIR6723 LOC101928626 LOC105378947
dgv2n14	Chr.1:629097 - 770988 on Build GRCh38	Gain	MTND2P28 OR4F16 MTND1P23 MIR6723 LOC107984841 LOC100133331 LOC100288069
esv21732	Chr.1:586033 - 788691 on Build GRCh38	Gain+Loss	MTND2P28 OR4F16 MTND1P23 MIR6723 LOC101928626 LOC107984841 LOC100287934 LOC105378947 LOC100133331 LOC100288069
nsv820617	Chr.1:629160 - 635395 on Build GRCh38	Duplication	MTND2P28 MTND1P23 MIR6723
nsv1003571	Chr.1:629393 - 863579 on Build GRCh38	Loss	LINC01128 MTND2P28 OR4F16 MTND1P23 MIR6723 LINC00115 LOC107984841 FAM87B LOC100287934 LOC100133331 LOC100288069

More Information

• Set Membership: Intergenic/Unknown, DGV Variation