BRCA1 mutation: genomic 3,835 bp deletion encompassing exon
- Number of haplotyped families = 5
- Numbers indicate linked allele in bp. When unambiguous phasing was not possible,
both alleles are given
- For marker details and methodology, see Peelen et al. (1997) A high
proportion of novel mutations in BRCA1 with strong founder effects among Dutch and
Belgian hereditary breast and ovarian cancer families.
Am. J. Hum. Genet. 60: 1041-1049.
- This deletion was described in detail by Petrij-Bosch et al. (1997) Nature
Genet. 17: 341-345.
|Family-ID ||Marker |
Last update: October 29, 1997