Observations with missing data will be deleted using listwise deletion at either the MDM creation stage or when the analysis is run.
One patient had a deletion at chromosome 14q22.1 involving the NIN gene.
Results showed that the sequence of GW2TD70 had a single nucleotide deletion at site 316 that generates a termination codon.
Self-directed lymphocytes may evade clonal deletion at ontogenesis but still remain harmless due to a mechanism called clonal anergy.
Eighteen Hsp70 promoter haplotypes were deduced, and seven of those haplotypes (n = 37) included the deletion at base 895.
A novel dCAPS marker was designed in accordance with a base A deletion at site 316 of the sequence.
A 1212-bp deletion at the qSW5 locus in Nipponbare was associated with an increase in the GW, as compared to Kasalath.
However, three accessions at the Jpn1 site showed genotypes without the deletion at all loci like Asian O. rufipogon, although they carried the meridionalis-type organellar genomes.
In the patient with deletion at 15q23 q24.1, the deletion overlapped with previously reported 15q24 deletion in ASD patients [27, 28].
Occasionally, the original information could arise again after a series of counteracting mutations, e.g., an insertion following a deletion at the same point.
Three alleles of qSW5/GW5 gene, Kasalath, indica II, and Nipponbare, were distinguished by length of deletion at the qSW5/GW5 locus (Yan et al. 2011).
