SMARCB1 MLPA


Description

MLPA using Kit 258-SMARCB1. this methodology will detect loss of heterozygosity of one or more exons in the SMARCB1 gene. Complemented by mutation detection of the SMARCB1 gene by bidirectional sequencing.

Also known as

INI1


Request a test

When requesting this test please use the referral form provided. Please also refer to any additional information provided for this test. Download the referral form >


Additional information

This MLPA kit detects loss of heterpzygosity of one or more exons of the SMARCB1 gene. It is used in conjunction with mutation detection of the SMARCB1 gene.


Sending address

Paediatric Malignancy Unit Great Ormond Street Hospital for Sick Children Level 2, Camelia Botnar Laboratories Great Ormond Street London WC1N 3JH

Laboratory service

Specialist Integrated Haematology and Malignancy Diagnostic Service- Acquired Genomics


Sample requirements

Fresh, frozen or FFPE tissue. If sending FFPE rolled tissue sections please send the equivalent of 80 uM of tissue.


Reference range

Not applicable


Turnaround time

40 working days


Disease / group

Rhabdoid tumours


Cost

Upon request


Call in advance?

Please call in advance to discuss requirements


Specialist Integrated Haematology and Malignancy Diagnostic Service- Acquired Genomics (SIHMDS-AG)

Specialist Integrated Haematology and Malignancy Diagnostic Service- Acquired Genomics (SIHMDS-AG) is a laboratory providing a wide range of molecular genetic and cytogenetic diagnostic tests.

© 2011 Great Ormond Street Hospital for Children NHS Trust