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1p11.2-q21.2CNV Type: Deletion


Largest CNV size: 26916336 bp

Statistics Box:
Number of Reports: 1



Summary Information

A de novo 1p11.2-q21.2 deletion was identified in a proband with Tourette syndrome in Wang et al., 2018.

Additional Locus Information

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USCS Symbol             NCBI Symbol

Decipher

            Decipher Symbol

References

Major Reports

Title
Author, Year
Report Class
CNV Type
De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis.
Deletion

Minor Reports

Title
Author, Year
Report Class
CNV Type

No Minor Reports

Cases

Cohort ID
Author, Year
Descripton
Cohort Size
Diagnosis
Age
Gender
CNV Size
Deletion
Duplication
Total CNV's
 wang_18_TS_discovery_cases
 Probands from 789 trio families (582 simplex trios, 103 multi-generational trios, and 104 trios with insufficient parental phenotypic data) from TIC Genetics, TAAICG, UTC, and TSGENESEE cohorts
 789
 Probands diagnosed with Tourette syndrome
 N/A
 80.57% Male
 26916336
 1
 0
 1

Controls

No Control Data Available

Cases

Cohort ID
Geographical Ancestry
Discovery Method
Platform
Algorithm
Software
Validation Method
 wang_18_TS_discovery_cases
  N/A
 WES
  Agilent SureSelect v1.1, Nimblegen EZ v2, Nimblegen EZ v3, IDT xGen
 
 CoNIFER
 qPCR

Controls

No Control Data Available

Cases

Patient ID
Author, Year
Age
Gender
Primary Diagnosis
Clinical Profile
Cognitive Profile
CNV Start
CNV End
CNV Size
Genome Build
Type Method
Validation
  wang_18_TS_discovery_cases-case25267.p1
 N/A
 N/A
 Tourette syndrome
 Tourette syndrome proband from phase 1 cohort; no additional clinical information available
 
 120324463
 149528945
  29204483
 GRCh38
 Deletion
 Yes

Controls

No Control Data Available

Cases

Patient ID
Validation Description
Primary Disorder Inheritence
Inheritence
Family Profile
Disease Segregation
Gene Content
Altered Gene Expression
 wang_18_TS_discovery_cases-case25267.p1
 qPCR
 
 De novo
 
 
 PFN1P2,RNVU1-19,PPIAL4A,RNVU1-4,HIST2H3DP1,RPL22P6,LINC01691,RNA5SP533,NKAIN1P1,PFN1P12,RNU1-114P,RNVU1-17,RNU1-92P,RNVU1-18,FAM91A3P,LINC02591,RNU1-143P,FCGR1CP,HIST2H3PS2,RPL22P5,IGKV1OR1-1,RNA5SP529,PPIAL4E,RNVU1-15,PFN1P6,PPIAL4F,RNA5SP59,PPIAL4D,RNVU1-14,NUDT17,MIR6736,RBM8A,GNRHR2,ANKRD34A,TXNIP,RNVU1-6,LINC01719,RNU6-1071P,NUDT4P2,RNA5SP536,PFN1P8,RNU1-151P,CCT8P1,RPL7AP15,OR13Z1P,OR13Z2P,OR13Z3P,RN7SL261P,GJA8,RNU1-129P,RNVU1-7,PDE4DIPP1,PFN1P4,ABHD17AP1,RNA5SP57,RNU1-120P,MIR5087,RNU1-122P,RNVU1-1,MIR6077,RNU1-13P,RNVU1-3,PPIAL4G,RNU6-1171P,NUDT4B,RN7SKP88,RNU2-38P,RNU1-59P,NBPF26,FCGR1B,FAM72B,EMBP1,NBPF17P,HIST2H2BB,FAM72C,DRD5P2,LINC01632,LINC01145,PFN1P3,NBPF25P,PDZK1,CD160,POLR3C,PIAS3,ITGA10,PEX11B,LIX1L-AS1,LIX1L,POLR3GL,HJV,NBPF10,NOTCH2NLA,SEC22B4P,NBPF12,NBPF13P,PRKAB2,PDIA3P1,CHD1L,ACP6,GJA5,PDZK1P1,LINC01731,SEC22B3,NBPF9,SEC22B2,NBPF8,LINC00623,HIST2H2BA,SRGAP2C,SRGAP2-AS1,SRGAP2D,NBPF15,SRGAP2B,FAM72D,NBPF20,GPR89A,ANKRD35,FMO5,LINC00624,BCL9,GPR89B,NBPF11,LINC01138,NBPF14,NBPF19,RNF115,HYDIN2,PDE4DIP
 

Controls

No Control Data Available
No Animal Model Data Available
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