accessibility menu, dialog, popup

UserName
Viewing profile as user:

Please enter the information below and press OK to send your cart to Core Services for purchase.

    

System Message

OKCancel
LOADING ...
Assay Reference Genome
Location

Chr.1:906834 on build GRCh38
Cytoband
1p36.33
Assay ID Hs03331200_cn
Size
Availability Made To Order
Catalog # 4400291
Price
Your Price
Online offer:
Check your price ›

Assay Details

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
dgv4n111 Chr.1:869076 - 914637 on Build GRCh38 Duplication FAM41C LOC284600
nsv1004962 Chr.1:629241 - 915295 on Build GRCh38 Gain FAM41C LOC284600 LOC100133331 LOC107984841 MIR6723 OR4F16 FAM87B MTND2P28 LOC100288069 LINC01128 LINC00115 LOC100287934 MTND1P23
nsv482937 Chr.1:10001 - 2368561 on Build GRCh38 Loss DDX11L1 LOC107984841 PRKCZ MIR6859-2 ATAD3B FAM87B MTND2P28 KLHL17 MIR429 MORN1 LINC00115 CCNL2 MIR1302-2 LOC100134822 WASH7P LOC729737 VWA1 TTLL10-AS1 ATAD3A TNFRSF4 MIR200B MIR6723 LOC100130417 NOC2L LOC102724312 SAMD11 FAM41C LOC284600 LOC100506504 MIR200A PERM1 TMEM88B UBE2J2 TNFRSF18 PUSL1 FAAP20 LOC102725121 MIR6727 DVL1 TTLL10 MIB2 TMEM240 FNDC10 GNB1 OR4F16 SCNN1D LOC105378949 OR4F29 CFAP74 FAM138A LOC100133331 AURKAIP1 MRPL20 ISG15 LOC148413 LOC100288069 C1orf159 LOC105378948 LOC105378592 LOC100287934 LOC105378591 LOC107985728 GABRD SKI HES4 CDK11A LOC100129534 SLC35E2 LOC107985729 SDF4 CPTP OR4F5 LOC100288175 LINC01342 CDK11B LOC100132287 TAS1R3 CALML6 MIR6808 MTND1P23 SSU72 LOC105378947 PLEKHN1 MIR6726 MXRA8 LOC101928626 ATAD3C NADK LOC105378589 MMP23B ACAP3 SLC35E2B MIR6859-1 RNF223 MMP23A FAM132A CPSF3L LINC01128 TMEM52 B3GALT6 AGRN ANKRD65
nsv950451 Chr.1:899421 - 1094520 on Build GRCh38 Deletion LOC284600 ISG15 KLHL17 PERM1 RNF223 LOC100130417 LOC100288175 C1orf159 NOC2L SAMD11 LOC105378948 PLEKHN1 LOC107985728 AGRN HES4
nsv509035 Chr.1:891406 - 985724 on Build GRCh38 Insertion NOC2L LOC284600 SAMD11 PLEKHN1 LOC107985728 KLHL17 PERM1 LOC100130417
dgv1n67 Chr.1:811028 - 914557 on Build GRCh38 Gain FAM41C LOC284600 LINC01128 LINC00115 FAM87B
nsv1005935 Chr.1:805477 - 915295 on Build GRCh38 Gain FAM41C LOC284600 LINC01128 LINC00115 FAM87B
esv3584981 Chr.1:837710 - 917284 on Build GRCh38 Loss FAM41C LOC284600 LINC01128 LOC100130417
nsv1009537 Chr.1:841742 - 915295 on Build GRCh38 Gain FAM41C LOC284600 LINC01128
nsv428334 Chr.1:874371 - 1220569 on Build GRCh38 Gain FAM41C LOC284600 MIR200A ISG15 KLHL17 PERM1 MIR429 C1orf159 LOC105378948 TNFRSF18 PLEKHN1 LOC107985728 HES4 TTLL10-AS1 TTLL10 TNFRSF4 MIR200B SDF4 RNF223 LOC100130417 LOC100288175 NOC2L LINC01342 SAMD11 AGRN
dgv5n100 Chr.1:585989 - 1114424 on Build GRCh38 Gain FAM41C LOC284600 LOC100133331 LOC107984841 LOC105378947 ISG15 FAM87B MTND2P28 KLHL17 PERM1 LOC100288069 C1orf159 LINC00115 LOC105378948 LOC100287934 PLEKHN1 LOC107985728 LOC101928626 HES4 MIR6723 OR4F16 RNF223 LOC100130417 LOC100288175 NOC2L LINC01128 SAMD11 MTND1P23 AGRN
nsv10161 Chr.1:776731 - 1777210 on Build GRCh38 Gain+Loss AURKAIP1 MRPL20 ISG15 ATAD3B FAM87B KLHL17 LOC148413 MIR429 LOC100288069 C1orf159 LINC00115 LOC105378948 LOC100287934 CCNL2 LOC107985728 HES4 VWA1 TTLL10-AS1 CDK11A ATAD3A TNFRSF4 SLC35E2 MIR200B LOC107985729 SDF4 CPTP LOC100130417 LOC100288175 NOC2L LINC01342 LOC102724312 CDK11B SAMD11 TAS1R3 MIR6808 SSU72 FAM41C LOC284600 MIR200A PERM1 TMEM88B UBE2J2 TNFRSF18 PUSL1 PLEKHN1 MIR6726 MXRA8 MIR6727 ATAD3C DVL1 TTLL10 NADK MMP23B MIB2 TMEM240 ACAP3 FNDC10 SLC35E2B SCNN1D RNF223 MMP23A FAM132A CPSF3L LINC01128 B3GALT6 AGRN ANKRD65
dgv1n111 Chr.1:690090 - 939522 on Build GRCh38 Duplication FAM41C LOC284600 LOC100133331 LOC107984841 OR4F16 FAM87B LOC100130417 LOC100288069 LINC01128 LINC00115 SAMD11 LOC100287934 LOC107985728
nsv517709 Chr.1:817186 - 1275912 on Build GRCh38 Gain+Loss FAM41C LOC284600 MIR200A ISG15 FAM87B KLHL17 PERM1 MIR429 C1orf159 LINC00115 LOC105378948 UBE2J2 TNFRSF18 PLEKHN1 LOC107985728 HES4 TTLL10-AS1 TTLL10 TNFRSF4 MIR200B SDF4 RNF223 LOC100130417 LOC100288175 FAM132A NOC2L LINC01342 LINC01128 SAMD11 B3GALT6 AGRN
dgv3n111 Chr.1:783283 - 939522 on Build GRCh38 Duplication FAM41C LOC284600 LINC01128 LINC00115 SAMD11 LOC100287934 FAM87B LOC107985728 LOC100130417
dgv2n67 Chr.1:877618 - 1426500 on Build GRCh38 Gain LOC284600 AURKAIP1 MRPL20 MIR200A ISG15 KLHL17 PERM1 LOC148413 MIR429 C1orf159 TMEM88B LOC105378948 CCNL2 UBE2J2 TNFRSF18 PUSL1 PLEKHN1 MIR6726 LOC107985728 MXRA8 MIR6727 HES4 TTLL10-AS1 DVL1 TTLL10 ACAP3 TNFRSF4 MIR200B SDF4 SCNN1D CPTP RNF223 LOC100130417 LOC100288175 FAM132A NOC2L CPSF3L LINC01342 SAMD11 TAS1R3 MIR6808 B3GALT6 AGRN ANKRD65
nsv832980 Chr.1:848279 - 1007037 on Build GRCh38 Gain NOC2L FAM41C LOC284600 LINC01128 SAMD11 PLEKHN1 LOC107985728 KLHL17 PERM1 LOC100130417 HES4
esv3584976 Chr.1:733250 - 914824 on Build GRCh38 Gain FAM41C LOC284600 LOC107984841 LINC01128 LINC00115 LOC100287934 FAM87B LOC100288069

Back To Top

More Information


Additional Information:

For this assay, SNP(s) [rs148658266] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Set Membership:

 Intergenic/Unknown DGV Variation

Back To Top

Related Products