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A study of reciprocal translocations and inversions detected by light microscopy with special reference to origin, segregation, and recurrent abnormalities

A study of reciprocal translocations and inversions detected by light microscopy with special reference to origin, segregation, and recurrent abnormalities
A study of reciprocal translocations and inversions detected by light microscopy with special reference to origin, segregation, and recurrent abnormalities
We analyzed 448 independently ascertained reciprocal translocations and 220 inversions referred to our diagnostic laboratory. Twenty-eight percent of the translocations and 8.5% of the inversions arose de novo, the proportion being influenced by the method of ascertainment. It was highest, 47%, among translocations ascertained through an abnormal phenotype. With the exception of the 3:1 unbalanced segregants, the remainders were equally likely to have been paternally or maternally inherited. The segregation from balanced translocation and inversion carriers showed an equal number of offspring with a normal chromosome constitution and with a balanced rearrangement. The number of unbalanced segregants among the translocations was 2.7% where the proband was balanced, and 19.2% where the proband was unbalanced. There was only a single unbalanced inversion. A search for recurring translocations showed only the well documented t(11;22) to occur with unusual frequency in our series and those of others, and we concluded that the few other translocations that were seen on more than one occasion were likely to be identical by descent (IBD). Similarly the majority of the recurring inversions, with the exception of common variants, seemed likely to be IBD. However, eight inversions recurred in our data and in most other series and may well be genuine independent rearrangements. A search of the known olfactory receptor (OR) loci and duplicons suggested that such sequences did not form an important contribution to the breakpoints of recurring rearrangements detected by light microscopy.
0148-7299
46 - 60
Youings, S.
ba64e5f7-1005-45ca-ba04-2ea40894b08a
Ellis, K.
0d30947b-3061-421d-8851-b8169b89ef9e
Ennis, S.
7b57f188-9d91-4beb-b217-09856146f1e9
Barber, J.
4785a6e4-bd63-4230-ab61-41a0ae12c761
Jacobs, P.
44a49fb2-53e9-428e-a20c-373b75e457f1
Youings, S.
ba64e5f7-1005-45ca-ba04-2ea40894b08a
Ellis, K.
0d30947b-3061-421d-8851-b8169b89ef9e
Ennis, S.
7b57f188-9d91-4beb-b217-09856146f1e9
Barber, J.
4785a6e4-bd63-4230-ab61-41a0ae12c761
Jacobs, P.
44a49fb2-53e9-428e-a20c-373b75e457f1

Youings, S., Ellis, K., Ennis, S., Barber, J. and Jacobs, P. (2004) A study of reciprocal translocations and inversions detected by light microscopy with special reference to origin, segregation, and recurrent abnormalities. American Journal of Medical Genetics part A, 126A (1), 46 - 60. (doi:10.1002/ajmg.a.20553).

Record type: Article

Abstract

We analyzed 448 independently ascertained reciprocal translocations and 220 inversions referred to our diagnostic laboratory. Twenty-eight percent of the translocations and 8.5% of the inversions arose de novo, the proportion being influenced by the method of ascertainment. It was highest, 47%, among translocations ascertained through an abnormal phenotype. With the exception of the 3:1 unbalanced segregants, the remainders were equally likely to have been paternally or maternally inherited. The segregation from balanced translocation and inversion carriers showed an equal number of offspring with a normal chromosome constitution and with a balanced rearrangement. The number of unbalanced segregants among the translocations was 2.7% where the proband was balanced, and 19.2% where the proband was unbalanced. There was only a single unbalanced inversion. A search for recurring translocations showed only the well documented t(11;22) to occur with unusual frequency in our series and those of others, and we concluded that the few other translocations that were seen on more than one occasion were likely to be identical by descent (IBD). Similarly the majority of the recurring inversions, with the exception of common variants, seemed likely to be IBD. However, eight inversions recurred in our data and in most other series and may well be genuine independent rearrangements. A search of the known olfactory receptor (OR) loci and duplicons suggested that such sequences did not form an important contribution to the breakpoints of recurring rearrangements detected by light microscopy.

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Published date: 1 April 2004
Organisations: Human Genetics

Identifiers

Local EPrints ID: 25052
URI: http://eprints.soton.ac.uk/id/eprint/25052
ISSN: 0148-7299
PURE UUID: d0aeaa24-1bcd-4749-af65-997e6ea66f3b
ORCID for S. Ennis: ORCID iD orcid.org/0000-0003-2648-0869

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Date deposited: 04 Apr 2006
Last modified: 16 Mar 2024 03:07

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Contributors

Author: S. Youings
Author: K. Ellis
Author: S. Ennis ORCID iD
Author: J. Barber
Author: P. Jacobs

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